Modulation of biological signal transduction by RNA interference

ABSTRACT

Compositions and methods relating to small interfering RNA (siRNA) polynucleotides are provided as pertains to modulation of biological signal transduction. Shown are siRNA polynucleotides that interfere with expression of members of the protein tyrosine phosphatase (PTP) class of enzymes that mediate signal transduction, and with certain MAP kinase kinases (MKK). In certain preferred embodiments siRNA modulate signal transduction pathways comprising SHP2, cdc14a/b, cdc25A/B/C, KAP, PTP-ε, PRL-3, CD45, dual specificity phosphatase-3 (DSP-3), MKK-4, and/or MKK-7. Modulation of PTP-mediated biological signal transduction has uses in diseases associated with defects in cell proliferation, cell differentiation and/or cell survival, such as metabolic disorders (including diabetes and obesity), cancer, autoimmune disease, infectious and inflammatory disorders and other conditions. The invention also provides siRNA polynucleotides that interfere with expression of chemotherapeutic target polypeptides, such as DHFR, thymidylate synthetase, and topoisomerase I.

CROSS-REFERENCE TO RELATED APPLICATION

[0001] This application claims the benefit of U.S. Provisional Patent Application No. 60/383,249 filed May 23, 2002, and U.S. Provisional Patent Application No. 60/462,942 filed Apr. 14, 2003, which are incorporated herein by reference in their entirety.

BACKGROUND OF THE INVENTION

[0002] 1. Technical Field

[0003] The present invention relates generally to compositions and methods useful for treating conditions associated with defects in cell proliferation, cell differentiation, and cell survival. The invention is more particularly related to double-stranded RNA polynucleotides that interfere with expression of protein tyrosine phosphatases, and polypeptide variants thereof. The invention is also particularly related to double-stranded RNA polynucleotides that interfere with expression of MAP kinases and MAP kinase kinases and chemotherapeutic target polypeptides, and polypeptide variants thereof. The present invention is also related to the use of such RNA polynucleotides to alter activation of signal transduction pathway components or to alter cellular metabolic processes that lead to proliferative responses, cell differentiation and development, and cell survival.

[0004] 2. Description of the Related Art

[0005] Reversible protein tyrosine phosphorylation, coordinated by the action of protein tyrosine kinases (PTKs) that phosphorylate certain tyrosine residues in polypeptides, and protein tyrosine phosphatases (PTPs) that dephosphorylate certain phosphotyrosine residues, is a key mechanism in regulating many cellular activities. It is becoming apparent that the diversity and complexity of the PTPs and PTKs are comparable, and that PTPs are equally important in delivering both positive and negative signals for proper function of cellular machinery. Regulated tyrosine phosphorylation contributes to specific pathways for biological signal transduction, including those associated with cell division, cell survival, apoptosis, proliferation and differentiation. Defects and/or malfunctions in these pathways may underlie certain disease conditions for which effective means for intervention remain elusive, including for example, malignancy, autoimmune disorders, diabetes, obesity and infection.

[0006] The protein tyrosine phosphatase (PTP) family of enzymes consists of more than 100 structurally diverse proteins in vertebrates, including almost 40 human PTPs that have in common the conserved 250 amino acid PTP catalytic domain, but which display considerable variation in their non-catalytic segments (Charbonneau and Tonks, 1992 Annu. Rev. Cell Biol. 8:463-493; Tonks, 1993 Semin. Cell Biol. 4:373-453; Andersen et al., Mol. Cell Biol. 21:7117-36 (2001)). This structural diversity presumably reflects the diversity of physiological roles of individual PTP family members, which in certain cases have been demonstrated to have specific functions in growth, development and differentiation (Desai et al., 1996 Cell 84:599-609; Kishihara et al., 1993 Cell 74:143-156; Perkins et al., 1992 Cell 70:225-236; Pingel and Thomas, 1989 Cell 58:1055-1065; Schultz et al., 1993 Cell 73:1445-1454). The PTP family includes receptor-like and non-transmembrane enzymes that exhibit exquisite substrate specificity in vivo and that are involved in regulating a wide variety of cellular signaling pathways (Andersen et al., Mol. Cell. Biol. 21:7117 (2001); Tonks and Neel, Curr. Opin. Cell Biol. 13:182 (2001)). PTPs thus participate in a variety of physiologic functions, providing a number of opportunities for therapeutic intervention in physiologic processes through alteration (i.e., a statistically significant increase or decrease) or modulation (e.g., up-regulation or down-regulation) of PTP activity.

[0007] Although recent studies have also generated considerable information regarding the structure, expression and regulation of PTPs, the nature of many tyrosine phosphorylated substrates through which the PTPs exert their effects remains to be determined. Studies with a limited number of synthetic phosphopeptide substrates have demonstrated some differences in the substrate selectivities of different PTPs (Cho et al., 1993 Protein Sci. 2: 977-984; Dechert et al., 1995 Eur. J. Biochem. 231:673-681). Analyses of PTP-mediated dephosphorylation of PTP substrates suggest that catalytic activity may be favored by the presence of certain amino acid residues at specific positions in the substrate polypeptide relative to the phosphorylated tyrosine residue (Salmeen et al., 2000 Molecular Cell 6:1401; Myers et al., 2001 J. Biol. Chem. 276:47771; Myers et al., 1997 Proc. Natl. Acad. Sci. USA 94:9052; Ruzzene et al., 1993 Eur. J. Biochem. 211:289295; Zhang et al., 1994 Biochemistry 33:2285-2290). Thus, although the physiological relevance of the substrates used in these studies is unclear, PTPs display a certain level of substrate selectivity in vitro.

[0008] The PTP family of enzymes contains a common evolutionarily conserved segment of approximately 250 amino acids known as the PTP catalytic domain. Within this conserved domain is a unique signature sequence motif, CX₅R (SEQ ID NO:______), that is invariant among all PTPs. In a majority of PTPs, an 11 amino acid conserved sequence ([IIV]HCXAGXXR[S/T)G (SEQ ID NO:______)) containing the signature sequence motif is found. The cysteine residue in this motif is invariant in members of the family and is essential for catalysis of the phosphotyrosine dephosphorylation reaction. It functions as a nucleophile to attack the phosphate moiety present on a phosphotyrosine residue of the incoming substrate. If the cysteine residue is altered by site-directed mutagenesis to serine (e.g., in cysteine-to-serine or “CS” mutants) or alanine (e.g., cysteine-to-alanine or “CA” mutants), the resulting PTP is catalytically deficient but retains the ability to complex with, or bind, its substrate, at least in vitro.

[0009] The CS mutant of one PTP, PTP1B (PTP-1B), is an example of such a PTP. Catalytically deficient mutants of such enzymes that are capable of forming stable complexes with phosphotyrosyl polypeptide substrates may be derived by mutating a wildtype protein tyrosine phosphatase catalytic domain invariant aspartate residue and replacing it with an amino acid that does not cause significant alteration of the Km of the enzyme but that results in a reduction in Kcat, as disclosed, for example, in U.S. Pat. Nos. 5,912,138 and 5,951,979, in U.S. application Ser. No. 09/323,426 and in PCT/US97/13016 and PCT/JUS00/14211. For instance, mutation of Asp 181 in PTP1B to alanine to create the aspartate-to-alanine (D to A or DA) mutant PTP1B-D181A results in a PTP1B “substrate trapping” mutant enzyme that forms a stable complex with its phosphotyrosyl polypeptide substrate (e.g., Flint et al., 1997 Proc. Natl. Acad. Sci. 94:1680). Substrates of other PTPs can be identified using a similar substrate trapping approach, for example substrates of the PTP family members PTP-PEST (Garton et al., 1996 J. Mol. Cell. Biol. 16:6408), TCPTP (Tiganis et al., 1998 Mol. Cell Biol. 18:1622), PTP-HSCF (Spencer et al., 1997 J. Cell Biol. 138:845), and PTP-H1 (Zhang et al., 1999 J. Biol. Chem. 274:17806).

[0010] Mitogen-activated protein kinases (MAP-kinases) are components of conserved cellular signal transduction pathways that have a variety of conserved members and that that are integral to the cell's response to stimuli such as growth factors, hormones, cytokines, and environmental stresses. MAP-kinases are activated by phosphorylation by MAP-kinase kinases at a dual phosphorylation motif that has the sequence Thr-X-Tyr, in which phosphorylation at the tyrosine and threonine residues is required for activity. Activated MAP-kinases phosphorylate several transduction targets, including effector protein kinases and transcription factors. Inactivation of MAP-kinases is mediated by dephosphorylation at the Thr-X-Tyr site by dual-specificity phosphatases referred to as MAP-kinase phosphatases. In higher eukaryotes, the physiological role of MAP-kinase signaling has been correlated with cellular events such as proliferation, oncogenesis, development, and differentiation. Accordingly, the ability to regulate signal transduction via these pathways could lead to the development of treatments and preventive therapies for human diseases associated with MAP-kinase signaling, such as cancer.

[0011] Dual-specificity protein tyrosine phosphatases (dual-specificity phosphatases) dephosphorylate both phosphotyrosine and phosphothreonine/serine residues (Walton et al., Ann. Rev. Biochem. 62:101-120, 1993). More than 50 dual-specificity phosphatases that dephosphorylate and inactivate a MAP-kinase have been identified (Shen et al., Proc. Natl. Acad. Sci. USA 98:13613-18 (2001)), including MKP-1 (WO 97/00315; Keyse and Emslie, Nature 59:644-647 (1992)); MKP-2 (WO97/00315); MKP-4, MKP-5, MKP-7, Hb5 (WO 97/06245); PAC1 (Ward et al., Nature 367:651-654 (1994)); HVH2 (Guan and Butch, J. Biol. Chem. 270:7197-7203 (1995)); and PYST1 (Groom et al., EMBO J. 15:3621-3632 (1996)). These dual-specificity phosphatases differ in expression, tissue and subcellular distribution, and specificity for MAP-kinase family members. Expression of certain dual-specificity phosphatases is induced by stress or mitogens, but others appear to be expressed constitutively in specific cell types. The regulation of dual-specificity phosphatase expression and activity is critical for control of MAP-kinase mediated cellular functions, including cell proliferation, cell differentiation and cell survival. For example, dual-specificity phosphatases may function as negative regulators of cell proliferation. It is likely that there are many such dual-specificity phosphatases, with varying specificity with regard to cell type or activation.

[0012] In contrast to the role of most dual-specificity phosphatases to inactivate MAP-kinases, one enzyme, herein referred to as dual-specificity phosphatase 3 (DSP-3), has been reported to have the capability to function as a selective activator of the JNK MAP-kinase signaling pathway (Shen et al., supra; WO 01/21812). DSP-3 appears also to affect the activity of other kinases involved in the JNK pathway (Shen et al., supra; WO 01/21812). For example, overexpression of DSP-3 leads to activation of MKK4, a MAP-kinase kinase that functions upstream of JNK (Shen et al., supra; Lawler et al., Curr. Biol. 8:1387-90 (1998); Yang et al., Proc. Natl. Acad. Sci. USA 94: 3004-3009 (1997)).

[0013] Activation of JNK is believed to be involved in several physiological processes, including embryonic morphogenesis, cell survival, and apoptosis. A number of JNK signaling pathway substrates have been identified, including c-Jun, ATF2, ELK-1 and others. JNK signaling has also been associated with various disease conditions, such as tumor development, ischemia and reperfusion injury, diabetes, hyperglycemia-induced apoptosis, cardiac hypertrophy, inflammation, and neurodegenerative disorders.

[0014] One non-transmembrane PTP, PTP1B, recognizes several tyrosine-phosphorylated proteins as substrates, many of which are involved in human disease. For example, therapeutic inhibition of PTP1B in the insulin signaling pathway may serve to augment insulin action, thereby ameliorating the state of insulin resistance common in Type II diabetes patients. PTP1B acts as a negative regulator of signaling that is initiated by several growth factor/hormone receptor PTKs, including p210 Bcr-Abl (LaMontagne et al., Mol. Cell Biol. 18:2965-75 (1998); LaMontagne et al., Proc. Natl. Acad. Sci. USA 95:14094-99 (1998)), receptor tyrosine kinases, such as EGF receptor, PDGF receptor, and insulin receptor (IR) (Tonks et al., Curr. Opin. Cell Biol. 13:182-95 (2001)), and JAK family members such as Jak2 and others (Myers et al., J. Biol. Chem. 276:47771-74 (2001)), as well as signaling events induced by cytokines (Tonks and Neel, 2001). Activity of PTP1B is regulated by modifications of several amino acid residues, such as phosphorylation of Ser residues (Brautigan and Pinault, 1993; Dadke et al., 2001; Flint et al., 1993), and oxidation of the active Cys residue in its catalytic motif (Lee et al., 1998; Meng et al., 2002) which is evolutionary conserved among protein tyrosine phosphatases and dual phosphatase family members (Andersen et al., 2001).

[0015] Disruption of the murine PTP1B gene homolog in a knock-out mouse model results in PTP1B^(−/−) mice exhibiting enhanced insulin sensitivity, decreased levels of circulating insulin and glucose, and resistance to weight gain even on a high-fat diet, relative to control animals having at least one functional PTP1B gene (Elchebly et al., Science 283:1544 (1999)). Insulin receptor hyperphosphorylation has also been detected in certain tissues of PTP1B deficient mice, consistent with a PTP1B contribution to the physiologic regulation of insulin and glucose metabolism (Id.). PTP-1B-deficient mice exhibit decreased adiposity (reduced fat cell mass but not fat cell number), increased basal metabolic rate and energy expenditure, and enhanced insulin-stimulated glucose utilization (Klaman et al., 2000 Mol. Cell. Biol. 20:5479). Additionally, altered PTP activity has been correlated with impaired glucose metabolism in other biological systems (e.g., McGuire et al., Diabetes 40:939 (1991); Myerovitch et al., J. Clin. Invest. 84:976 (1989); Sredy et al., Metabolism 44:1074 (1995)), including PTP involvement in biological signal transduction via the insulin receptor (see, e.g., WO 99/46268 and references cited therein).

[0016] An integration of crystallographic, kinetic, and PTP1B-peptide binding assays illustrated the interaction of PTP1B and insulin receptor (IR) (Salmeen et al., Mol. Cell 6:1401-12 (2000)). The insulin receptor (IR) comprises two extracellular α subunits and two transmembrane β subunits. Activation of the receptor results in autophosphorylation of tyrosine residues in both β subunits, each of which contains a protein kinase domain. Extensive interactions that form between PTP1B and insulin receptor kinase (IRK) encompass tandem pTyr residues at 1162 and 1163 of IRK, such that pTyr-1162 is located in the active site of PTP1B (id.). The Asp/Glu-pTyr-pTyr-Arg/Lys motif has been implicated for optimal recognition by PTP1B for IRK. This motif is also present in other receptor PTKs, including Trk, FGFR, and Axl. In addition, this motif is found in the JAK family of PTKs, members of which transmit signals from cytokine receptors, including a classic cytokine receptor that is recognized by the satiety hormone leptin (Touw et al., Mol. Cell. Endocrinol. 160:1-9 (2000)).

[0017] Changes in the expression levels of PTP1B have been observed in several human diseases, particularly in diseases associated with disruption of the normal patterns of tyrosine phosphorylation. For example, the expression of PTP1B is induced specifically by the p210 Bcr-Abl oncoprotein, a PTK that is directly responsible for the initial manifestations of chronic myelogenous leukemia (CML) (LaMontagne et al., Mol. Cell. Biol. 18:2965-75 (1998); LaMontagne et al., Proc. Natl. Acad. Sci. USA 95:14094-99 (1998)). Expression of PTPB1 in response to this oncoprotein is regulated, in part, by transcription factors Sp1, Sp3, and Egr-1 (Fukada et al., J. Biol. Chem. 276:25512-19 (2001)). These transcription factors have been shown to bind to a p210 Bcr-Abl responsive sequence (PRS) in the human PTP1B promoter, located between 49 to −37 base pairs from the transcription start site, but do not appear to mediate certain additional, independent PTP1B transcriptional events, for which neither transcription factor(s) nor transcription factor recognition element(s) have been defined (id.).

[0018] Diabetes mellitus is a common, degenerative disease affecting 5-10% of the human population in developed countries, and in many countries, it may be one of the five leading causes of death. Approximately 2% of the world's population has diabetes, the overwhelming majority of cases (>97%) being type 2 diabetes and the remainder being type 1. In type 1 diabetes, which is frequently diagnosed in children or young adults, insulin production by pancreatic islet beta cells is destroyed. Type 2 diabetes, or “late onset” or “adult onset” diabetes, is a complex metabolic disorder in which cells and tissues cannot effectively use available insulin; in some cases insulin production is also inadequate. At the cellular level, the degenerative phenotype that may be characteristic of late onset diabetes mellitus includes, for example, impaired insulin secretion and decreased insulin sensitivity, i.e., an impaired response to insulin.

[0019] Studies have shown that diabetes mellitus may be preceded by or is associated with certain related disorders. For example, an estimated forty million individuals in the U.S. suffer from late onset impaired glucose tolerance (IGT). IGT patients fail to respond to glucose with increased insulin secretion. Each year a small percentage (5-10%) of IGT individuals progress to insulin deficient non-insulin dependent diabetes (NIDDM). Some of these individuals further progress to insulin dependent diabetes mellitus (IDDM). NIDDM and IDDM are associated with decreased release of insulin by pancreatic beta cells and/or a decreased response to insulin by cells and tissues that normally exhibit insulin sensitivity. Other symptoms of diabetes mellitus and conditions that precede or are associated with diabetes mellitus include obesity, vascular pathologies, and various neuropathies, including blindness and deafness.

[0020] Type 1 diabetes is treated with lifelong insulin therapy, which is often associated with undesirable side effects such as weight gain and an increased risk of hypoglycemia. Current therapies for type 2 diabetes (NIDDM) include altered diet, exercise therapy, and pharmacological intervention with injected insulin or oral agents that are designed to lower blood glucose levels. Examples of such presently available oral agents include sulfonylureas, biguanides, thiazolidinediones, repaglinide, and acarbose, each of which alters insulin and/or glucose levels. None of the current pharmacological therapies, however, controls the disease over its full course, nor do any of the current therapies correct all of the physiological abnormalities in type 2 NIDDM, such as impaired insulin secretion, insulin resistance, and excessive hepatic glucose output. In addition, treatment failures are common with these agents, such that multi-drug therapy is frequently necessary.

[0021] In certain metabolic diseases or disorders, one or more biochemical processes, which may be either anabolic or catabolic (e.g., build-up or breakdown of substances, respectively), are altered (e.g., increased or decreased in a statistically significant manner) or modulated (e.g., up- or down-regulated to a statistically significant degree) relative to the levels at which they occur in a disease-free or normal subject such as an appropriate control individual. The alteration may result from an increase or decrease in a substrate, enzyme, cofactor, or any other component in any biochemical reaction involved in a particular process. Altered (i.e., increased or decreased in a statistically significant manner relative to a normal state) PTP activity can underlie certain disorders and suggests a PTP role in certain metabolic diseases.

[0022] RNA interference (RNAi) is a polynucleotide sequence-specific, post-transcriptional gene silencing mechanism effected by double-stranded RNA that results in degradation of a specific messenger RNA (mRNA), thereby reducing the expression of a desired target polypeptide encoded by the mRNA (see, e.g., WO 99/32619; WO 01/75164; U.S. Pat. No. 6,506,559; Fire et al., Nature 391:806-11 (1998); Sharp, Genes Dev. 13:139-41 (1999); Elbashir et al. Nature 411:494-98 (2001); Harborth et al., J. Cell Sci. 114:4557-65 (2001)). RNAi is mediated by double-stranded polynucleotides as also described hereinbelow, for example, double-stranded RNA (dsRNA), having sequences that correspond to exonic sequences encoding portions of the polypeptides for which expression is compromised. RNAi reportedly is not effected by double-stranded RNA polynucleotides that share sequence identity with intronic or promoter sequences (Elbashir et al., 2001). RNAi pathways have been best characterized in Drosophila and Caenorhabditis elegans, but “small interfering RNA” (siRNA) polynucleotides that interfere with expression of specific polypeptides in higher eukaryotes such as mammals (including humans) have also been considered (e.g., Tuschl, 2001 Chembiochem. 2:239-245; Sharp, 2001 Genes Dev. 15:485; Bernstein et al., 2001 RNA 7:1509; Zamore, 2002 Science 296:1265; Plasterk, 2002 Science 296:1263; Zamore 2001 Nat. Struct. Biol. 8:746; Matzke et al., 2001 Science 293:1080; Scadden et al., 2001 EMBO Rep. 2:1107).

[0023] According to a current non-limiting model, the RNAi pathway is initiated by ATP-dependent, processive cleavage of long dsRNA into double-stranded fragments of about 18-27 (e.g., 19, 20, 21, 22, 23, 24, 25, 26, etc.) nucleotide base pairs in length, called small interfering RNAs (siRNAs) (see review by Hutvagner et al., Curr. Opin. Gen. Dev. 12:225-32 (2002); Elbashir et al., 2001; Nykänen et al., Cell 107:309-21 (2001); Zamore et al., Cell 101:25-33 (2000); Bass, Cell 101:235-38 (2000)). In Drosophila, an enzyme known as “Dicer” cleaves the longer double-stranded RNA into siRNAs; Dicer belongs to the RNase III family of dsRNA-specific endonucleases (WO 01/68836; Bernstein et al., Nature 409:363-66 (2001)). Further according to this non-limiting model, the siRNA duplexes are incorporated into a protein complex, followed by ATP-dependent unwinding of the siRNA, which then generates an active RNA-induced silencing complex (RISC) (WO 01/68836). The complex recognizes and cleaves a target RNA that is complementary to the guide strand of the siRNA, thus interfering with expression of a specific protein (Hutvagner et al., supra).

[0024] In C. elegans and Drosophila, RNAi may be mediated by long double-stranded RNA polynucleotides (WO 99/32619; WO 01/75164; Fire et al., 1998; Clemens et al., Proc. Natl. Acad. Sci. USA 97:6499-6503 (2000); Kisielow et al., Biochem. J. 363:1-5 (2002); see also WO 01/92513 (RNAi-mediated silencing in yeast)). In mammalian cells, however, transfection with long dsRNA polynucleotides (i.e., greater than 30 base pairs) leads to activation of a non-specific sequence response that globally blocks the initiation of protein synthesis and causes mRNA degradation (Bass, Nature 411:428-29 (2001)). Transfection of human and other mammalian cells with double-stranded RNAs of about 18-27 nucleotide base pairs in length interferes in a sequence-specific manner with expression of particular polypeptides encoded by messenger RNAs (mRNA) containing corresponding nucleotide sequences (WO 01/75164; Elbashir et al., 2001; Elbashir et al., Genes Dev. 15:188-200 (2001)); Harborth et al., J. Cell Sci. 114:4557-65 (2001); Carthew et al., Curr. Opin. Cell Biol. 13:244-48 (2001); Mailand et al., Nature Cell Biol. Advance Online Publication (Mar. 18, 2002); Mailand et al. 2002 Nature Cell Biol. 4:317).

[0025] siRNA polynucleotides may offer certain advantages over other polynucleotides known to the art for use in sequence-specific alteration or modulation of gene expression to yield altered levels of an encoded polypeptide product. These advantages include lower effective siRNA polynucleotide concentrations, enhanced siRNA polynucleotide stability, and shorter siRNA polynucleotide oligonucleotide lengths relative to such other polynucleotides (e.g., antisense, ribozyme or triplex polynucleotides). By way of a brief background, “antisense” polynucleotides bind in a sequence-specific manner to target nucleic acids, such as mRNA or DNA, to prevent transcription of DNA or translation of the mRNA (see, e.g., U.S. Pat. No. 5,168,053; U.S. Pat. No. 5,190,931; U.S. Pat. No. 5,135,917; U.S. Pat. No. 5,087,617; see also, e.g., Clusel et al., 1993 Nuc. Acids Res. 21:3405-11, describing “dumbbell” antisense oligonucleotides). “Ribozyme” polynucleotides can be targeted to any RNA transcript and are capable of catalytically cleaving such transcripts, thus impairing translation of mRNA (see, e.g., U.S. Pat. No. 5,272,262; U.S. Pat. No. 5,144,019; and U.S. Pat. Nos. 5,168,053, 5,180,818, 5,116,742 and 5,093,246; U.S. 2002/193579). “Triplex” DNA molecules refers to single DNA strands that bind duplex DNA to form a colinear triplex molecule, thereby preventing transcription (see, e.g., U.S. Pat. No. 5,176,996, describing methods for making synthetic oligonucleotides that bind to target sites on duplex DNA). Such triple-stranded structures are unstable and form only transiently under physiological conditions. Because single-stranded polynucleotides do not readily diffuse into cells and are therefore susceptible to nuclease digestion, development of single-stranded DNA for antisense or triplex technologies often requires chemically modified nucleotides to improve stability and absorption by cells. siRNAs, by contrast, are readily taken up by intact cells, are effective at interfering with the expression of specific polypeptides at concentrations that are several orders of magnitude lower than those required for either antisense or ribozyme polynucleotides, and do not require the use of chemically modified nucleotides.

[0026] Importantly, despite a number of attempts to devise selection criteria for identifying oligonucleotide sequences that will be effective in siRNA based on features of the desired target mRNA sequence (e.g., percent GC content, position from the translation start codon, or sequence similarities based on an in silico sequence database search for homologues of the proposed siRNA) it is presently not possible to predict with any degree of confidence which of myriad possible candidate siRNA sequences that can be generated as nucleotide sequences that correspond to a desired target mRNA (e.g., dsRNA of about 18-27 nucleotide base pairs) will in fact exhibit siRNA activity (i.e., interference with expression of the polypeptide encoded by the mRNA). Instead, individual specific candidate siRNA polynucleotide or oligonucleotide sequences must be generated and tested to determine whether interference with expression of a desired polypeptide target can be effected. Accordingly, no routine method exists in the art for designing a siRNA polynucleotide that is, with certainty, capable of specifically altering the expression of a given PTP polypeptide, and thus for the overwhelming majority of PTPs no effective siRNA polynucleotide sequences are presently known.

[0027] Currently, therefore, desirable goals for therapeutic regulation of biological signal transduction include modulation of PTP (e.g., PTP-1B, DSP-3, SHP-2, KAP, PRL-3, cdc14 or cdc25 or other PTP)-mediated cellular events include, inter alia, inhibition or potentiation of interactions among PTP-binding molecules, substrates and binding partners, or of other agents that regulate PTP activities. Accordingly, a need exists in the art for an improved ability to intervene in the regulation of phosphotyrosine signaling, including regulating PTPs by altering PTP catalytic activity, PTP binding to PTP substrate molecules, and/or PTP-encoding gene expression. An increased ability to so regulate PTPs may facilitate the development of methods for modulating the activity of proteins involved in phosphotyrosine signaling pathways and for treating conditions associated with such pathways. The present invention fulfills these needs and further provides other related advantages.

SUMMARY OF THE INVENTION

[0028] Briefly stated, the present invention provides siRNA compositions and methods for modulating biological signal transduction. In one aspect the present invention provides isolated small interfering RNA (siRNA) polynucleotide, comprising at least one nucleotide sequence selected from the sequences set forth in SEQ ID NOS: 4-7, 100-103, 105-108, 120-123, 125-128, 130-133, 140-143, 145-148, 150-153, 440-443, 445-448, 455-458, 460-463, 465-468, 470-473, 475-478, 480-483, 485-488, or 490-493, and the complementary polynucleotide thereto. The small interfering RNA polynucleotide is capable of interfering with expression of a polypeptide, which polypeptide comprises an amino acid sequence as set forth in a sequence SEQ ID NO: 779, SEQ ID NO 789, SEQ ID NO 791, SEQ ID NO 797, SEQ ID NO 799, SEQ ID NO 801, SEQ ID NO 803, SEQ ID NO 805, SEQ ID NO 807, SEQ ID NO 809, SEQ ID NO 811, or SEQ ID NO 813.

[0029] In certain embodiments, the nucleotide sequence of the siRNA polynucleotide differs by one, two, three or four nucleotides at any of positions 1-19 of a sequence selected from the sequences set forth in SEQ ID NOS: 4-7, 100-103, 105-108, 120-123, 125-128, 130-133, 140-143, 145-148, 150-153, 440-443, 445-448, 455-458, 460-463, 465-468, 470-473, 475-478, 480-483, 485-488, or 490-493. In other embodiments, the nucleotide sequence of the siRNA polynucleotide differs by at least two, three or four nucleotides at any of positions 1-19 of a sequence selected from the sequences set forth in SEQ ID NOS: 4-7, 100-103, 105-108, 120-123, 125-128, 130-133, 140-143, 145-148, 150-153, 440-443, 445-448, 455-458, 460-463, 465-468, 470-473, 475-478, 480-483, 485-488, or 490-493. In particular embodiments the invention provides an isolated siRNA polynucleotide comprising a nucleotide sequence selected from SEQ ID NOS: 4, or the complement thereof; from SEQ ID NOS: 100, 105, or the complement thereof; from SEQ ID NOS: 120, 125, or 130; or the complement thereof, from SEQ ID NOS: 140, 145, or 150, or the complement thereof; from SEQ ID NOS: 440 or 445, or the complement thereof; from SEQ ID NOS: 455 or 460; from SEQ ID NO: 465, or the complement thereof; from SEQ ID NOS: 470 or 475, or the complement thereof; from SEQ ID NOS: 480, 485, or 490, or the complement thereof.

[0030] In certain embodiments the invention provides the above siRNA polynucleotides that comprise at least one synthetic nucleotide analogue of a naturally occurring nucleotide. In certain other embodiments, the siRNA polynucleotide is linked to a detectable label, wherein the detectable label is a reporter molecule. In particular embodiments, the reporter molecule is a dye, a radionuclide, a luminescent group, a fluorescent group, or biotin. In other particular embodiments, the fluorescent group is fluorescein isothiocyanate and in other particular embodiments, the detectable label is a magnetic particle.

[0031] The invention also provides a pharmaceutical composition comprising an siRNA polynucleotide selectted from the sequences set forth in SEQ ID NOS: 4-7, 100-103, 105-108, 120-123, 125-128, 130-133, 140-143, 145-148, 150-153, 440-443, 445-448, 455-458, 460-463, 465-468, 470-473, 475-478, 480-483, 485-488, or 490-493, and a physiologically acceptable carrier. In particular embodiments, the the carrier comprises a liposome.

[0032] The invention also provides a recombinant nucleic acid construct comprising a polynucleotide that is capable of directing transcription of a small interfering RNA (siRNA), the polynucleotide comprising: (i) a first promoter; (ii) a second promoter; and (iii) at least one DNA polynucleotide segment comprising at least one nucleotide sequence selected from SEQ ID NOS: 4-7, 100-103, 105-108, 120-123, 125-128, 130-133, 140-143, 145-148, 150-153, 440-443, 445-448, 455-458, 460-463, 465-468, 470-473, 475-478, 480-483, 485-488, or 490-493, or a complement thereto, wherein each DNA polynucleotide segment and its complement are operably linked to at least one of the first and second promoters, and wherein the promoters are oriented to direct transcription of the DNA polynucleotide segment and its reverse complement. In certain embodiments, the recombinant nucleic acid construct comprises at least one enhancer that is selected from a first enhancer operably linked to the first promoter and a second enhancer operably linked to the second promoter. In certain other embodiments, the recombinant nucleic acid construct comprises at least one transcriptional terminator that is selected from (i) a first transcriptional terminator that is positioned in the construct to terminate transcription directed by the first promoter and (ii) a second transcriptional terminator that is positioned in the construct to terminate transcription directed by the second promoter. The invention also provides that the siRNA transcribed from the recombinant nucleic acid construct is capable of interfering with expression of a polypeptide, wherein the polypeptide comprises an amino acid sequence as set forth in a sequence selected from SEQ ID NO: 779, SEQ ID NO 789, SEQ ID NO 791, SEQ ID NO 797, SEQ ID NO 799, SEQ ID NO 801, SEQ ID NO 803, SEQ ID NO 805, SEQ ID NO 807, SEQ ID NO 809, SEQ ID NO 811, or SEQ ID NO 813.

[0033] The present invention also provides a recombinant nucleic acid construct comprising a polynucleotide that is capable of directing transcription of a small interfering RNA (siRNA), the polynucleotide comprising at least one promoter and a DNA polynucleotide segment, wherein the DNA polynucleotide segment is operably linked to the promoter, and wherein the DNA polynucleotide segment comprises (i) at least one DNA polynucleotide that comprises at least one nucleotide sequence selected from SEQ ID NOS: 4-7, 100-103, 105-108, 120-123, 125-128, 130-133, 140-143, 145-148, 150-153, 440-443, 445-448, 455-458, 460-463, 465-468, 470-473, 475-478, 480-483, 485-488, or 490-493, or a complement thereto; (ii) a spacer sequence comprising at least 4 nucleotides operably linked to the DNA polynucleotide of (i); and (iii) the reverse complement of the DNA polynucleotide of (i) operably linked to the spacer sequence. In certain embodiments, the siRNA polynucleotide transcribed from the recombinant nucleic acid construct comprises an overhang of at least one and no more than four nucleotides, the overhang being located immediately 3′ to (iii). In certain particular embodiments, the spacer sequence comprises at least 9 nucleotides. In certain other specific embodiments the spacer sequence comprises two uridine nucleotides that are contiguous with (iii). In one embodiment, the recombinant nucleic acid construct comprises at least one transcriptional terminator that is operably linked to the DNA polynucleotide segment. The invention also provides a host cell that is transformed or transfected with such a recombinant nucleic acid construct as disclosed herein.

[0034] In one embodiment, the invention provides a pharmaceutical composition comprising an siRNA polynucleotide and a physiologically acceptable carrier, wherein the siRNA polynucleotide is selected from (i) an RNA polynucleotide that comprises at least one nucleotide sequence selected from SEQ ID NOS: 4-7, 100-103, 105-108, 120-123, 125-128, 130-133, 140-143, 145-148, 150-153, 440-443, 445-448, 455-458, 460-463, 465-468, 470-473, 475-478, 480-483, 485-488, or 490-493; (ii) an RNA polynucleotide that comprises at least one nucleotide sequence selected from SEQ ID NOS: 4-7, 100-103, 105-108, 120-123, 125-128, 130-133, 140-143, 145-148, 150-153, 440-443, 445-448, 455-458, 460-463, 465-468, 470-473, 475-478, 480-483, 485-488, or 490-493, and the complementary polynucleotide thereto; (iii) an RNA polynucleotide according to (i) or (ii) wherein the nucleotide sequence of the siRNA polynucleotide differs by one, two or three nucleotides at any of positions 1-19 of a sequence selected from SEQ ID NOS: 4-7, 100-103, 105-108, 120-123, 125-128, 130-133, 140-143, 145-148, 150-153, 440-443, 445-448, 455-458, 460-463, 465-468, 470-473, 475-478, 480-483, 485-488, or 490-493, or (iv) an RNA polynucleotide according to (i) or (ii) wherein the nucleotide sequence of the siRNA polynucleotide differs by two, three or four nucleotides at any of positions 1-19 of a sequence selected from the sequences set forth in SEQ ID NOS: 4-7, 100-103, 105-108, 120-123, 125-128, 130-133, 140-143, 145-148, 150-153, 440-443, 445-448, 455-458, 460-463, 465-468, 470-473, 475-478, 480-483, 485-488, or 490-493. In certain particular embodiments, the physiologically acceptable carrier comprises a liposome.

[0035] The present invention also provides a method for interfering with expression of a polypeptide, or variant thereof, comprising contacting a subject that comprises at least one cell which is capable of expressing the polypeptide with a siRNA polynucleotide for a time and under conditions sufficient to interfere with expression of the polypeptide, wherein: (a) the polypeptide comprises an amino acid sequence as set forth in a sequence selected from SEQ ID NO: 779, SEQ ID NO 789, SEQ ID NO 791, SEQ ID NO 797, SEQ ID NO 799, SEQ ID NO 801, SEQ ID NO 803, SEQ ID NO 805, SEQ ID NO 807, SEQ ID NO 809, SEQ ID NO 811, or SEQ ID NO 813, (b) the siRNA polynucleotide is selected from (i) an RNA polynucleotide which comprises at least one nucleotide sequence selected from SEQ ID NOS: 4-7, 100-103, 105-108, 120-123, 125-128, 130-133, 140-143, 145-148, 150-153, 440-443, 445-448, 455-458, 460-463, 465-468, 470-473, 475-478, 480-483, 485-488, or 490-493, (ii) an RNA polynucleotide that comprises at least one nucleotide sequence selected from the group consisting of SEQ ID NOS: 4-7, 100-103, 105-108, 120-123, 125-128, 130-133, 140-143, 145-148, 150-153, 440-443, 445-448, 455-458, 460-463, 465-468, 470-473, 475-478, 480-483, 485-488, or 490-493, and the complementary polynucleotide thereto, (iii) an RNA polynucleotide according to (i) or (ii) wherein the nucleotide sequence of the siRNA polynucleotide differs by one, two or three nucleotides at any of positions 1-19 of a sequence selected from SEQ ID NOS: 4-7, 100-103, 105-108, 120-123, 125-128, 130-133, 140-143, 145-148, 150-153, 440-443, 445-448, 455-458, 460-463, 465-468, 470-473, 475-478, 480-483, 485-488, or 490-493, or (iv) an RNA polynucleotide according to (i) or (ii) wherein the nucleotide sequence of the siRNA polynucleotide differs by two, three or four nucleotides at any of positions 1-19 of a sequence selected from the group consisting of the sequences set forth in SEQ ID NOS: 4-7, 100-103, 105-108, 120-123, 125-128, 130-133, 140-143, 145-148, 150-153, 440-443, 445-448, 455-458, 460-463, 465-468, 470-473, 475-478, 480-483, 485-488, or 490-493.

[0036] In another embodiment, the invention provides a method for interfering with expression of a polypeptide that comprises an amino acid sequence as set forth in a sequence selected from SEQ ID NO: 779, SEQ ID NO 789, SEQ ID NO 791, SEQ ID NO 797, SEQ ID NO 799, SEQ ID NO 801, SEQ ID NO 803, SEQ ID NO 805, SEQ ID NO 807, SEQ ID NO 809, SEQ ID NO 811, or SEQ ID NO 813, or a variant of said polypeptide, said method comprising contacting, under conditions and for a time sufficient to interfere with expression of the polypeptide, (i) a subject that comprises at least one cell that is capable of expressing the polypeptide, and (ii) a recombinant nucleic acid construct according to the present invention as described herein.

[0037] In another embodiment, the invention provides a method for identifying a component of a signal transduction pathway comprising: (A) contacting a siRNA polynucleotide and a first biological sample comprising at least one cell that is capable of expressing a target polypeptide, or a variant of said polypeptide, under conditions and for a time sufficient for target polypeptide expression when the siRNA polynucleotide is not present, wherein (i) the target polypeptide comprises an amino acid sequence as set forth in a sequence selected from SEQ ID NO: 779, SEQ ID NO 789, SEQ ID NO 791, SEQ ID NO 797, SEQ ID NO 799, SEQ ID NO 801, SEQ ID NO 803, SEQ ID NO 805, SEQ ID NO 807, SEQ ID NO 809, SEQ ID NO 811, SEQ ID NO 813, SEQ ID NO 823, SEQ ID NO 825, or SEQ ID NO:827; (2) the siRNA polynucleotide is selected from (i) an RNA polynucleotide which comprises at least one nucleotide sequence selected from SEQ ID NOS: 4-7, 100-103, 105-108, 120-123, 125-128, 130-133, 140-143, 145-148, 150-153, 440-443, 445-448, 455-458, 460-463, 465-468, 470-473, 475-478, 480-483, 485-488, or 490-493, (ii) an RNA polynucleotide that comprises at least one nucleotide sequence selected from SEQ ID NOS: 4-7, 100-103, 105-108, 120-123, 125-128, 130-133, 140-143, 145-148, 150-153, 440-443, 445-448, 455-458, 460-463, 465-468, 470-473, 475-478, 480-483, 485-488, or 490-493, and the complementary polynucleotide thereto; (iii) an RNA polynucleotide according to (i) or (ii) wherein the nucleotide sequence of the siRNA polynucleotide differs by one, two or three nucleotides at any of positions 1-19 of a sequence selected from the group consisting of the sequences set forth in SEQ ID NOS: 4-7, 100-103, 105-108, 120-123, 125-128, 130-133, 140-143, 145-148, 150-153, 440-443, 445-448, 455-458, 460-463, 465-468, 470-473, 475-478, 480-483, 485-488, or 490-493, (iv) an RNA polynucleotide according to (i) or (ii) wherein the nucleotide sequence of the siRNA polynucleotide differs by two, three or four nucleotides at any of positions 1-19 of a sequence selected from the group consisting of the sequences set forth in SEQ ID NOS: 4-7, 100-103, 105-108, 120-123, 125-128, 130-133, 140-143, 145-148, 150-153, 440-443, 445-448, 455-458, 460-463, 465-468, 470-473, 475-478, 480-483, 485-488, or 490-493; and (B) comparing a level of phosphorylation of at least one protein that is capable of being phosphorylated in the cell with a level of phosphorylation of the protein in a control sample that has not been contacted with the siRNA polynucleotide, wherein an altered level of phosphorylation of the protein in the presence of the siRNA polynucleotide relative to the level of phosphorylation of the protein in an absence of the siRNA polynucleotide indicates that the protein is a component of a signal transduction pathway. The invention also provides a small interfering RNA (siRNA) polynucleotide, comprising an RNA polynucleotide which comprises at least one nucleotide sequence selected from SEQ ID NOS:4-7, 100-103, 105-108, 120-123, 125-128, 130-133, 140-143, 145-148, 150-153, 440-443, 445-448, 455-458, 460-463, 465-468, 470-473, 475-478, 480-483, 485-488, or 490-493. Certain further embodiments relate to isolated siRNA polynucleotides that comprise nucleotide sequences having the above recited SEQ ID NOS, including compositions and methods for producing and therapeutically using such siRNA.

[0038] These and other embodiments of the present invention will become apparent upon reference to the following detailed description and attached drawings. All references disclosed herein are hereby incorporated by reference in their entireties as if each was incorporated individually. Also incorporated by reference are co-pending application Ser. No. ______ and Ser. No. ______ (attorney docket numbers 200125.441 and 200125.448, respectively), which have been filed concurrently.

BRIEF DESCRIPTION OF THE DRAWINGS

[0039]FIG. 1 presents an immunoblot analysis of the expression of MKP-1 polypeptide in HeLa cells co-transfected with sequence-specific siRNA polynucleotides (MKPsi.1 (MKP.1, SEQ ID NO:______), lanes 1-3; MKPsi.2 (MKP.2, SEQ ID NO:______), lanes 4-6) and a non-specific sequence siRNA (CD45si.1, lanes 7-9). The immunoblot of HeLa cell extracts was probed with an anti-MKP-1 antibody (upper). A second SDS-PAGE gel in which the HeLa cell extracts were separated was stained with Coomassie Blue (lower).

[0040]FIG. 2 shows an immunoblot analysis of 292-HEK cell lysates from cells co-transfected with FLAG®-DSP-11, FLAG®-DSP-18, FLAG®-DSP-3, and FLAG®-cdc14b expression vectors and siRNAs specific for DSP-11 or DSP-18. The presence of each polypeptide was detected using an anti-FLAG® antibody (Sigma-Aldrich, St. Louis, Mo.). The upper immunoblot shows the level of expression of FLAG®-DSP-11 in untransfected 293-HEK cells (lane 1); 293-HEK cells transfected with FLAG®-DSP-11 vector DNA only (buffer) (lane 2), siRNA DSP11.2 (lane 3), siRNA DSP11.4 (lane 4), siRNA DSP18.2 (lane 5), and siRNA DSP18.2 (lane 6); and the level of expression of 293-HEK cells transfected with FLAG®-DSP-18 vector DNA only (buffer) (lane 7); 293-HEK cells co-transfected with siRNA DSP11.2 (lane 8), siRNA DSP11.4 (lane 9), siRNA DSP18.2 (lane 10), and siRNA DSP18.2 (lane 11). The lower immunoblot shows the level of FLAG®-DSP-3 in untransfected 293-HEK cells (lane 1); 293-HEK cells transfected with FLAG®-DSP-3 vector DNA only (buffer) (lane 2); 293-HEK cells co-transfected with siRNA DSP11.2 (lane 3), siRNA DSP11.4 (lane 4), siRNA DSP18.2 (lane 5), and siRNA DSP18.2 (lane 6); and the level of expression of FLAG®-cdc14b in 293-HEK cells transfected with FLAG®-cdc14b vector DNA only (buffer) (lane 7); 293-HEK cells co-transfected with siRNA DSP11.2 (lane 8), siRNA DSP11.4 (lane 9), siRNA DSP18.2 (lane 10), and siRNA DSP18.2 (lane 11).

[0041]FIG. 3 shows the effect on JNK activation by sequence-specific siRNA interference of DSP-3 polypeptide expression. HeLa cells were co-transfected with a DSP-3 recombinant expression vector and DSP3.1 siRNA (SEQ ID NO:1) or 60 pmoles (100 nM final) CD45.2 (SEQ ID NO:______). After transfection, cells were stimulated with either tumor necrosis factor-alpha (TNF-α) or epidermal growth factor (EGF) or were unstimulated (Unstim.).

[0042]FIG. 4 shows the effect on JNK activation by sequence-specific siRNA interference of DSP-3 polypeptide expression. HeLa cells were co-transfected with a DSP-3 recombinant expression vector and DSP3.1 siRNA (SEQ ID NO:______) or 60 pmoles (100 nM final) CD45.2 (SEQ ID NO:______). After transfection, cells were stimulated with sorbitol.

[0043]FIG. 5 presents an immunoblot analysis of ERK phosphorylation in HeLa cells co-transfected with a DSP-3 recombinant expression vector and DSP-3 specific siRNA DSP3.1, non-specific CD45.2 siRNA, or siRNA annealing buffer and then stimulated with TNF-α, EGF, sorbitol, and anisomycin. Lane 1: unstimulated cells transfected with DSP3.1 siRNA; lane 2: unstimulated cells transfected with CD45.2 siRNA; lane 3: cells transfected with DSP3.1 siRNA and stimulated with TNF-α; lane 4: cells transfected with CD45.2 siRNA and stimulated with TNF-α; lane 5: cells transfected with DSP3.1 siRNA and stimulated with EGF; lane 6: cells transfected with CD45.2 siRNA and stimulated with EGF; lane 7: unstimulated cells transfected with CD45.2 siRNA; lane 8: unstimulated cells transfected with siRNA annealing buffer; lane 9: cells transfected with DSP3.1 siRNA and stimulated with sorbitol; lane 10: cells transfected with CD45.2 siRNA and stimulated with sorbitol; lane 11; cells transfected with siRNA annealing buffer and stimulated with sorbitol; lane 12: cells transfected with DSP3.1 siRNA and stimulated with anisomycin; lane 13: cells transfected with CD45.2 siRNA and stimulated with anisomycin; lane 14: cells transfected with siRNA annealing buffer and stimulated with anisomycin.

[0044]FIG. 6 shows an immunoblot analysis of FLAG®-tagged cdc14a expression in 293-HEK cells co-transfected with cdc14a.2 (lane 3); cdc14a.3 (lane 4); cdc14a.4 (land 5); cdc14a.5 (lane 6); DSP3.1 (lane 7); DSP3.2 (lane 8); cdc14b.3 (lane 9); cdc14b.4 (lane 10); MKP.2 (lane 11); CD45.3 (lane 12); no siRNA (lane 2). Untransfected cells were prepared as a control (lane 1). Expression was detected using an anti-FLAG® antibody (Sigma-Aldrich).

[0045]FIG. 7 presents an immunoblot of expression of FLAG®-tagged dual specificity phosphatases in 293-HEK cells that were co-transfected with cdc14a.3 siRNA (denoted by +). Lanes 2 and 3: expression of FLAG®-tagged cdc14a; lanes 4 and 5: expression of FLAG®-tagged DSP-3; lanes 6 and 7: expression of FLAG®-tagged cdc14b; lanes 8 and 9: FLAG®-tagged DSP-11. The immunoblot to the right is an over-exposure of the immunoblot on the left to detect low concentrations of expressed polypeptides.

[0046]FIG. 8 shows an immunoblot analysis of FLAG®-tagged cdc14b expression in 293-HEK cells co-transfected with cdc14b.3 (lane 3); cdc14b.4 (lane 4); cdc14a.3 (land 5); cdc14a.5 (lane 6); DSP3.1 (lane 7); DSP3.2 (lane 8); MKP.2 (lane 9); CD45.3 (lane 10); no siRNA (lane 2). Untransfected cells were prepared as a control (lane 1). Expression was detected using an anti-FLAG® antibody (Sigma-Aldrich).

[0047]FIG. 9 presents an immunoblot of expression of FLAG®-tagged dual specificity phosphatases in 293-HEK cells co-transfected with either cdc14a or cdc14b specific siRNAs. Expression of the phosphatases was detected with an anti-FLAG® antibody. 293-HEK cells were transfected as follows: no expression vector or siRNA (lane 1); FLAG®-tagged cdc14b only (lane 2); FLAG®-tagged cdc14b and cdc14b.3 siRNA (lane 3); FLAG®-tagged cdc14b and cdc14b.4 (lane 5); FLAG®-tagged DSP-3 only (lane 5); FLAG®-tagged DSP-3 and cdc14b.3 siRNA (lane 6); FLAG®-tagged DSP3 and cdc14b.4 siRNA (lane 7); FLAG®-tagged DSP-3 and cdc14a.5 siRNA (lane 8); FLAG®-tagged DSP-11 only (lane 9); FLAG®-tagged DSP-11 and cdc14b.3 siRNA (land 10); FLAG®-tagged DSP-11 and cdc14b.4 siRNA (lane 11); and FLAG®-tagged DSP-11 and cdc14a.5 siRNA.

[0048]FIG. 10 depicts the expression of cdc14b polypeptide in HeLa cells co-transfected with cdc14b.4 siRNA detected by immunocytochemistry (top right, 10× magnification; bottom right, 40× magnification) and in the absence of a specific siRNA (top left, 10× magnification; bottom right, 40× magnification).

[0049]FIG. 11 depicts an immunoblot of the effect on endogenous expression of murine PTP1B by siRNAs specific for the murine PTP1B or the human PTP1B polynucleotide sequences. Expression was detected using a murine anti-PTP1B monoclonal antibody. Data are presented for two different clones of C57B16 #3 murine cells. Both clones were transfected with mPTP1B1.1 siRNA (lanes 3 and 8); MPTP1B1.2 (lanes 4 and 9); mPTP1B1.3 (lanes 5 and 10). One clone, C57B16 #3 clone 3, was transfected with hPTP1B1.1 (lane 6). Lane 2: untransfected C57B16 #3, clone 3; lane 7: untransfected C57B16 #3, clone 10.

[0050]FIG. 12 presents an extended consensus cDNA sequence encoding prototypical DSP-18 (DSP-18pr) (FIG. 12A) [SEQ ID NO:______] and the deduced DSP-18pr amino acid sequence (FIG. 12B) [SEQ ID NO:______]. In FIG. 12A, initiating methionine (ATG) and stop (TGA) codons and intron/exon splice junctions are depicted in bold type with the splice donor sequences in bold without underscore, and the splice acceptor sequences in bold with underscore. In FIG. 12B, initiating methionine and the phosphatase active site are depicted in bold type.

[0051]FIG. 13 presents nucleotide and amino acid sequences for a DSP-18 isoform, DSP-18a. FIG. 13A presents a cDNA sequence for DSP-18a [SEQ ID NO:______], with the start (ATG) and stop (TGA) codons and intron/exon splice junctions indicated in bold; intron/exon splice junctions are depicted in bold type with the splice donor sequences in bold without underscore and the splice acceptor sequences in bold with underscore. FIG. 13B presents the amino acid sequence of the DSP-18a polypeptide [SEQ ID NO:______] encoded by SEQ ID NO:______, with the phosphatase active site depicted in bold type.

[0052]FIG. 14 presents nucleotide and amino acid sequences for a DSP-18 isoform, DSP-18b. FIG. 14A presents a cDNA sequence for DSP-18b [SEQ ID NO:______], with the start (ATG) and stop (TGA) codons and intron/exon splice junctions indicated in bold; intron/exon splice junctions are depicted in bold type with the splice donor sequences in bold without underscore and the splice acceptor sequences in bold with underscore. FIG. 14B presents the amino acid sequence of the DSP-18b polypeptide [SEQ ID NO:______] encoded by SEQ ID NO:______, with the phosphatase active site depicted in bold type.

[0053]FIG. 15 presents nucleotide sequences for DSP-18 isoforms, DSP-18c and DSP-18d. FIG. 15A presents a cDNA sequence for DSP-18c [SEQ ID NO:______ with the start (ATG) and stop (TGA) codons and intron/exon splice junctions indicated in bold. FIG. 15B presents a cDNA sequence for DSP-18d [SEQ ID NO:______], with the start (ATG) and stop (TGA) codons and intron/exon splice junctions indicated in bold. DSP-18c [SEQ ID NO:______] encoded by SEQ ID NO:______, and DSP-18d [SEQ ID NO:______] encoded by SEQ ID NO:______, both share the 181 amino acid sequence encoded by the open reading frame of DSP-18a (see FIG. 15).

[0054]FIG. 16 presents nucleotide and amino acid sequences for DSP-18 isoforms, DSP-18e and DSP-18f. FIG. 16A presents a cDNA sequence for DSP-18e [SEQ ID NO:______], with the start (ATG) and stop (TGA) codons and intron/exon splice junctions indicated in bold. FIG. 16 presents the amino acid sequence of DSP-18e polypeptide [SEQ ID NO:______] encoded by SEQ ID NO:______, with the phosphatase active site sequence in boldface type.

[0055]FIG. 17A presents nucleotide and amino acid sequences for DSP-18f. FIG. 17A presents a cDNA sequence for DSP-18f [SEQ ID NO:______], with the start (ATG) and stop (TGA) codons and intron/exon splice junctions indicated in bold. FIG. 17B presents the amino acid sequence of DSP-18f polypeptide [SEQ ID NO:______] encoded by SEQ ID NO:______, with the phosphatase active site sequence in boldface type.

[0056]FIG. 18 represents an immunoblot of cleavage of poly(ADP-ribose) polymerase (PARP) in HeLa cells transfected with cell division cycle protein sequence specific siRNA polynucleotides (10 nM). The upper immunoblot was probed with an antibody that specifically binds to cleaved PARP, and the lower immunoblot was probed with an anti-PARP antibody. The siRNA polynucleotides transfected into the HeLa cells were as follows: lanes 1 and 2, no siRNA; lanes 3 and 4, cdc14a.5; lanes 5 and 6, cdc14b.4; lanes 7 and 8 Cdc25A.2; lanes 9 and 10, Cdc25B.4; and lanes 11 and 12, Cdc25C.1.

[0057]FIG. 19 depicts an immunoblot analysis of the expression of human PTP-1 B co-transfected into 1BKO+HIR murine fibroblasts with human PTP-1B siRNA hairpin vectors. Expression was detected with an anti-human PTP1B antibody (h1B) (lower portion of immunoblot). As a protein expression control, cell lysates were probed with an anti-human insulin receptor (IR) antibody (upper portion of immunoblot).

[0058]FIG. 20 illustrates insulin-induced activation of PKB/Akt in HepG2 cells following ablation of TC45 by RNA interference. FIG. 20A represents an immunoblot of serum-deprived Rat-1 and HEPG2 cells that were exposed to varying concentrations of insulin (INS) as shown. The insulin receptor (IR) was immunoprecipitated from cell lysates with an anti-IR-β antibody followed by immunoblotting with an anti-phosphotyrosine antibody (pY) (top panel); an anti-pYpY^(1162/1163)-IR-β antibody (middle panel); and an anti-IR β antibody. FIG. 20B represents an immunoblot of HepG2 cell lysates prepared from cells that were untransfected (control) or transfected with TCPTP1 siRNA (SEQ ID NO:______) (+siRNA). The lysates were immunoblotted with an anti-phospho-PKB/Akt antibody (p-AKT) (first immunoblot); anti-PKB/Akt antibody (AKT) (second immunoblot); anti-TC45 (TC45) antibody (third immunoblot); and an anti-PTP1B antibody (PTP1B). FIG. 20C represents a densitometric analysis of the gel image to illustrate the ratio of phosphorylated PKB/Akt to total PKB/Akt.

[0059]FIG. 21 provides an immunoblot indicating that tyrosine phosphorylated IR-β is a substrate of TC45. HepG2 cells overexpressing wild-type (WT) or substrate trapping mutant (DA) forms of PTP1B (1B) and TC45 were either not treated with insulin (−INS) or stimulated with insulin for 5 minutes (+INS), lysed, separated by SDS-PAGE, and immunoprecipitated with anti-PTP1B antibody (FG6) or anti-TC45 antibody (CF4). The immunoprecipitates were immunoblotted with an anti-IR-β antibody (top panel, FIG. 21A); anti-PTP1B antibody FG6 (middle panel, FIG. 21A); and anti-TCPTP antibody CF4 (bottom panel, FIG. 21A). FIG. 21B depicts immunoblots of HepG2 cells that were serum-starved and untransfected (control) or transfected with TC45 siRNA (100 nM) and then stimulated with 10 nM insulin (INS) for the indicated times. The insulin receptor was immunoprecipitated from cell lysates with an anti-IR-β antibody, which was then immunoblotted with the following antibodies: anti-phosphotyrosine (p-Tyr) (first immunoblot); anti-pY⁹⁷²-IR-β (second immunoblot); anti-pYpY^(1162/1163)-IR-β (third immunoblot); and anti-IR-β (fourth immunoblot). FIG. 21C presents densitometric analyses of the gel image to show the ratio of phosphorylated IR-β to total IR-β for total phosphotyrosine (top panel); phosphorylation of Tyr 972 (middle panel); and phosphorylation of the activation loop tyrosines 1162 and 1163 (lower panel).

[0060]FIG. 22 presents the results of an ELISA in which the level of insulin receptor (IR) phosphorylated tyrosine was measured in 293-HEK HIR cells transfected with 0, 0.5, 3, or 10 nM hPTP1B1.3 (H1.3, SEQ ID NO:______) (FIG. 22A) or mPTP1B1.1b (M1.1, SEQ ID NO:______) (FIG. 22B) siRNAs. The level of expression of human PTP1B in the cells was compared by immunoblot (see tables to right of each figure).

[0061]FIG. 23 depicts the results of an ELISA in which the level of insulin receptor (IR) phosphorylated tyrosine was measured in 293-HEK HIR cells transfected with 0, 0.5, 3, or 10 nM siRNAs. The siRNA polynucleotides transfected into the cells included hPTP1B1.2 (H1.2, SEQ ID NO:______); hPTP1B1.3 (H1.3, SEQ ID NO:______); mPTP1B1.1b (M1.1, SEQ ID NO:______); and rPTP1B1.2 (R1.2, SEQ ID NO:______). Seventy-two hours after transfection, cells were exposed to insulin for 7 minutes at the designated concentrations. Cell lysates were prepared and coated onto 96-well plates and probed with an anti-pY-IR-β antibody.

[0062]FIG. 24 depicts the results of an ELISA in which the level of insulin receptor (IR) phosphorylated tyrosine was measured in 293-HEK HIR cells transfected with 0, 0.5, 3, or 10 nM hTCPTP1.4 siRNA (TC1.4, SEQ ID NO:______) (FIG. 24A) and mPTP1B1.1b siRNA (M1.1, SEQ ID NO:______) (FIG. 24B). Seventy-two hours after transfection, cells were exposed to insulin for 7 minutes at the designated concentrations. Cell lysates were prepared and coated onto 96-well plates and probed with an anti-pY-IR-β antibody.

[0063]FIG. 25 represents ELISA data from three separate experiments that represent the level of insulin receptor phosphorylation in cells transfected with hPTP1B1.3 and stimulated with 50 nM insulin (Ins). Each data point represents the average optical density measured in duplicate wells.

[0064]FIG. 26 illustrates an MTT assay comparing proliferation of HCT-116 cells transfected with siRNAs specific for DSP-3 (dsp3.1 (SEQ ID NO:______) and dsp3.4 (SEQ ID NO:______)); cdc14a (a.3 (SEQ ID NO:______) and a.5 (SEQ ID NO:______)); SHP-2 (shp2.1 (SEQ ID NO:______) and shp2.2 (SEQ ID NO:______); and DHFR (DHFR.1 (SEQ ID NO:______). As a control, HCT-116 cells were transfected with nonspecific siRNA (scr.2 (SEQ ID NO:______)). Each bar represents the average optical density for six wells.

[0065]FIG. 27 illustrates an MTT assay comparing proliferation of T47D cells transfected with siRNAs specific for DSP-3 (dsp3.1 (SEQ ID NO:______) and dsp3.4 (SEQ ID NO:______)); cdc14a (Cdc14a.3 (SEQ ID NO:______) and Cdc14a.5 (SEQ ID NO:______); SHP-2 (shp2.1 (SEQ ID NO:______) and shp2.2 (SEQ ID NO:______); and DHFR (DHFR.1 (SEQ ID NO:______). As a control, T47D cells were transfected with nonspecific siRNA (scr.2 (SEQ ID NO:______).

[0066]FIG. 28 represents an immunoblot of cleavage of PARP in HCT-116 cells (FIG. 28A) and T47D (FIG. 28B) transfected with buffer only (lane 1); (scrb1.2 (SEQ ID NO:______) (lane 2); DSP3.1 (SEQ ID NO:______) (lane 3); DSP3.4 (SEQ ID NO:______) (lane 4); and DHFR.1 (lane 5).

[0067]FIG. 29 presents nucleotide and amino acid sequences for DSP-13. FIG. 29A presents a cDNA sequence for DSP-13 [SEQ ID NO:______], with the start (ATG) and stop (TGA) codons indicated in bold and underlined. FIG. 29B presents the amino acid sequence of the DSP-13 polypeptide [SEQ ID NO:______] encoded by SEQ ID NO:______.

[0068]FIG. 30 presents nucleotide and amino acid sequences for DSP-14. FIG. 30A presents a cDNA sequence for DSP-14 [SEQ ID NO:______], with the start (ATG) and stop (TGA) codons indicated in bold and underlined. FIG. 30B presents the amino acid sequence of the DSP-14 polypeptide [SEQ ID NO:______] encoded by SEQ ID NO:______.

DETAILED DESCRIPTION OF THE INVENTION

[0069] The present invention is directed in part to the unexpected discovery of short RNA polynucleotide sequences that are capable of specifically modulating expression of a desired polypeptide, such as a DSP-3, SHP-2, KAP, PRL-3, cdc14 or cdc25 polypeptide, or a variant of any such polypeptide. Without wishing to be bound by theory, the RNA polynucleotides of the present invention specifically reduce expression of a desired target polypeptide through recruitment of small interfering RNA (siRNA) mechanisms. In particular, and as described in greater detail herein, according to the present invention there are provided compositions and methods that relate to the surprising identification of certain specific RNAi oligonucleotide sequences of 19, 20, 21, 22, 23, 24, 25, 26 or 27 nucleotides that can be derived from corresponding polynucleotide sequences encoding the desired DSP-3, SHP-2, KAP, PRL-3, cdc14, cdc25, or other specified target polypeptide. These sequences cannot be predicted through any algorithm, sequence alignment routine, or other systematic paradigm, but must instead be obtained through generation and functional testing for RNAi activity of actual candidate oligonucleotides, such as those disclosed for the first time herein.

[0070] In preferred embodiments of the invention, the siRNA polynucleotide interferes with expression of a DSP-3, SHP-2, KAP, PRL-3, cdc14, cdc25, or other herein specified target polypeptide or a variant thereof, and comprises a RNA oligonucleotide or RNA polynucleotide uniquely corresponding in its nucleotide base sequence to the sequence of a portion of a target polynucleotide encoding the target polypeptide, for instance, a target mRNA sequence or an exonic sequence encoding such mRNA. Hence, according to non-limiting theory, the siRNA polynucleotides of the present invention direct sequence-specific degradation of mRNA encoding a desired DSP-3, SHP-2, KAP, PRL-3, cdc14 or cdc25 target polypeptide, the expression of which is consequently compromised. As also described herein, certain embodiments of the invention relate to siRNA polynucleotides that specifically interfere with expression of PTPs that are dual specificity phosphatases, including DSP-3, DSP-11, DSP-13, DSP-14, and DSP-18; certain other embodiments relate to RNAi interference with expression of the MAP kinase kinase (MKK) target polypeptide MKK4; certain other embodiments relate to RNAi interference with expression of target polypeptides that interact with chemotherapeutic agents, for example, the target polypeptides dihydrofolate reductase (DHFR), thymidylate synthetase, and topoisomerase I. The invention relates in preferred embodiments to siRNA polynucleotides that interfere with expression of specific polypeptides in mammals, which in certain particularly preferred embodiments are humans and in certain other particularly preferred embodiments are non-human mammals.

[0071] Exemplary sequences for the target polypeptides described herein include, for instance, DSP-3 (WO 00/60092; SEQ ID NO:24 encoded by SEQ ID NO:23); cdc14A (e.g., GenBank Accession Nos. AF122013, AF064102, AF064103; Li et al., 1997 J. Biol. Chem. 272:29403; U.S. Pat. No. 6,331,614; e.g., SEQ ID NO:34 encoded by SEQ ID NO:33) or cdc14B (e.g., GenBank Accession Nos. AF064104, AF064105, AF023158; Li et al., 1997 J. Biol. Chem. 272:29403; e.g., SEQ ID NO:36 encoded by SEQ ID NO:35); cdc25A ((e.g., GenBank Accession Nos. NM_(—)001789, AF527417, NM_(—)133571); cdc25B (e.g., GenBank Accession Nos. NM_(—)133572, NM_(—)023117, NM_(—)021872; NM_(—)021872; M81934); and cdc25C (e.g., GenBank Accession Nos. NM_(—)001790, NM_(—)022809); PTPε (e.g., Genbank Accession Nos. NM_(—)006504 (SEQ ID NOS: ______-______) and NM_(—)130435(SEQ ID NOS: ______-______)); KAP (e.g., Genbank Accession No. L27711; Hannon et al., Proc. Natl. Acad. Sci. USA 91:1731-35 (1994); Demetrick et al., Cytogenet. Cell Genet. 69:190-92 (1995)); PRL-3 (e.g., Zhao et al., Genomics 35:172-81 (1996); Genbank Accession Nos. (NM_(—)003479 (SEQ ID NOS: ______-______), NM_(—)080392 (SEQ ID NOS: ______-______), NM_(—)080391 (SEQ ID NOS: ______-______), NM_(—)032611 (SEQ ID NOS: ______-______), and NM_(—)007079 (SEQ ID NOS: ______-______); SHP-2 (GenBank Accession Nos. D13540 (SEQ ID NOS: ______-______); L03535 (SEQ ID NOS: ______-______); L07527 (SEQ ID NOS: ______-______); X70766 (SEQ ID NOS: ______-______); L08807 (SEQ ID NO: ______); 78088 (SEQ ID NOS: ______-______); S39383 (SEQ ID NO: ______); D84372 (SEQ ID NOS: ______-______); U09307 (SEQ ID NOS: ______-______); CD45 (e.g., (Charbonneau et al., Proc. Natl. Acad. Sci. USA 85:7182-86 (1988); Genbank Accession Nos. NM_(—)080922 (SEQ ID NOS: ______-______), NM_(—)080921 (SEQ ID NOS: ______-______), NM_(—)002838 (SEQ ID NOS: ______-______), and NM_(—)080923) (SEQ ID NOS: ______-______); GenBank Ace. No. XM_(—)16748; e.g., SEQ ID NO:32 encoded by SEQ ID NO:31); SEQ ID NOS:______-______); DSP-11 (WO 01/05983, SEQ ID NO:26 encoded by SEQ ID NO:25); DSP-18 (U.S. application Ser. No. 10/151,320, SEQ ID NO:28 encoded by SEQ ID NO:27); DSP-13 (U.S. application Ser. No. 09/775,925; SEQ ID NO:______ encoded by SEQ ID NO:______); DSP-14 (U.S. application Ser. No. 09/847,519; SEQ ID NO:______ encoded by SEQ ID NO:______); WO 01/46394); MKP-1 (WO 97/00315; Keyse et al., 1992 Nature 59:644; SEQ ID NO:30 encoded by SEQ ID NO:29). According to the contemplated invention, the siRNA polynucleotide expressly does not consist of a CDC14a.5 polynucleotide having a sequence set forth in SEQ ID NO:10 (Mailand et al., 2002 Nature Cell Biol. 4:317).

[0072] In certain embodiments of the invention, an siRNA polynucleotide interferes with expression of a component of a signaling transduction pathway, for example, components of the JNK signaling transduction pathway such as MKK4 (e.g., GenBank Accession Nos. L36870 (SEQ ID NO:______ and ______), NM_(—)009157, and NM_(—)009157; SEQ ID NO: ______ encoded by SEQ ID NO: ______)) and MKK7 (e.g., GenBank Accession Nos. AF013588 (SEQ ID NO: ______ encoded by SEQ ID NO:______) and AF026216, and to related compositions and methods. (See also Shen et al., Proc. Natl. Acad. Sci. USA 98:13613-18 (2001)). In certain other embodiments of the invention, the siRNA polynucleotide interferes with expression of a cellular polypeptide or enzyme that is associated with a cellular malfunction or defect (e.g., in a cancer or malignancy, an enzyme that is overexpressed or constitutively expressed and is associated with cell survival, proliferation, apoptosis, cell division, and differentiation). For example, the siRNA polynucleotide may comprise a sequence specific for dihydrofolate reductase (DHFR) (e.g., GenBank Accession No: NM_(—)000791; SEQ ID NO: ______ encoded by SEQ ID NO:______)); thymidylate synthetase e.g., GenBank Accession No: NM_(—)001071 (SEQ ID NO: ______ encoded by SEQ ID NO:______); topoisomerase I (e.g., GenBank Accession No: J03250; SEQ ID NO: ______ encoded by SEQ ID NO:______)); IkappaB kinase (IKK) alpha (e.g., GenBank Accession No. AF080157; SEQ ID NO: ______ encoded by SEQ ID NO:______); GenBank Accession No. AF009225; GenBank Accession No. AF012890); IKKbeta e.g., GenBank Accession No. AF080158; SEQ ID NO: ______ encoded by SEQ ID NO:______); GenBank Accession No. AF031416; GenBank Accession No. AF029684); or IKKgamma e.g., GenBank Accession No. AF074382; SEQ ID NO: ______ encoded by SEQ ID NO:______); GenBank Accession No. AF091453).

[0073] In another preferred embodiment, the siRNA polynucleotides provided interfere with expression of DSP-3, SHP-2, CD45, PTPε, KAP, cdc14a, cdc14b, cdc25A, cdc25B, cdc25C, and PRL-3. According to non-limiting theory, the siRNA polynucleotides of the present invention direct sequence-specific degradation of mRNA encoding a PTP such as SHP2, PTPε, or a dual specificity phosphatase (e.g., DSP-3, KAP, cdc14a, cdc14b, cdc25A, cdc25B, cdc25C, CD45, or PRL-3) by a mechanism known as RNA interference (RNAi). The invention is not intended, however, to be so limited, and certain embodiments relate to RNA interference of other PTPs and dual specificity phosphatases (e.g., DSP-11, DSP-13, DSP-14, and DSP-18), and to interference with expression of other polypeptides and components of signal transduction pathways including mitogen activated protein (MAP) kinases, which include a MAP kinase kinase (e.g., MAPKKK or MEKK) that activates a MAP/ERK kinase (e.g., MAPKK or MEK), which then stimulates a phosphorylation-dependent increase in the activity of the MAP kinase. Upon activation, a MAP kinase can phosphorylate a variety of intracellular targets including transcription factors, transcriptional adaptor proteins, membrane and cytoplasmic substrates, and other protein kinases. In certain preferred embodiments, a siRNA polynucleotide interferes with expression of a MAP kinase kinase that is a component of the JNK signal transduction pathway, for example, MKK4 or MKK7. In other preferred embodiments, a siRNA polynucleotide interferes with expression of a cellular polypeptide or enzyme that is associated with a cellular malfunction or defect in cancer or malignancy, and which may be overexpressed or constitutively expressed in the tumor cell.

[0074] In addition, other preferred polypeptides include polypeptides that are targets of chemotherapeutic agents or drugs. Examples of chemotherapeutic target polypeptides include enzymes in the folate metabolic pathway, for example, thymidylate synthetase, which is a target of fluoropyrmidines. Another enzyme in this pathway is dihydrofolate reductase (DHFR), which is targeted by antifolate agents, such as methotrexate. DNA processing enzymes, including topoisomerase I and topoisomerase II, are also targets of chemotherapeutic agents. Other examples of chemotherapeutic target polypeptides include microtubule polypeptides, which are chemotherapeutic targets of taxanes and vinca alkaloids. According to non-limiting theory, these chemotherapeutic target polypeptides may become resistant to a drug or agent, that is, resistance may be manifested by overexpression or constitutive expression of the chemotherapeutic target polypeptide in a target cell. The overexpression of such a target polypeptide may be reduced by introducing a specific siRNA polynucleotide into the cell. In certain embodiments of the invention, a siRNA polynucleotide interferes with expression of such chemotherapeutic target polypeptides. For example, siRNA polynucleotides of the present invention that interfere with expression of a chemotherapeutic target polypeptide comprise sequences specific for dihydrofolate reductase (DHFR), thymidylate synthetase, topoisomerase I, and IKKgamma.

[0075] SiRNA Polynucleotides

[0076] As used herein, the term “siRNA” means either: (i) a double stranded RNA oligonucleotide, or polynucleotide, that is 18 base pairs, 19 base pairs, 20 base pairs, 21 base pairs, 22 base pairs, 23 base pairs, 24 base pairs, 25 base pairs, 26 base pairs, 27 base pairs, 28 base pairs, 29 base pairs or 30 base pairs in length and that is capable of interfering with expression and activity of a PTP-1B polypeptide, or a variant of the PTP-1B polypeptide, wherein a single strand of the siRNA comprises a portion of a RNA polynucleotide sequence that encodes the PTP-1B polypeptide, its variant, or a complementary sequence thereto; (ii) a single stranded oligonucleotide, or polynucleotide of 18 nucleotides, 19 nucleotides, 20 nucleotides, 21 nucleotides, 22 nucleotides, 23 nucleotides, 24 nucleotides, 25 nucleotides, 26 nucleotides, 27 nucleotides, 28 nucleotides, 29 nucleotides or 30 nucleotides in length and that is either capable of interfering with expression and/or activity of a target polypeptide such as DSP-3, SHP-2, KAP, PRL-3, cdc14 or cdc25, or a variant of the target polypeptide, or that anneals to a complementary sequence to result in a dsRNA that is capable of interfering with target polypeptide expression, wherein such single stranded oligonucleotide comprises a portion of a RNA polynucleotide sequence that encodes the target polypeptide, its variant, or a complementary sequence thereto; or (iii) an oligonucleotide, or polynucleotide, of either (i) or (ii) above wherein such oligonucleotide, or polynucleotide, has one, two, three or four nucleic acid alterations or substitutions therein.

[0077] A siRNA polynucleotide is a RNA nucleic acid molecule that mediates the effect of RNA interference, a post-transcriptional gene silencing mechanism. A siRNA polynucleotide preferably comprises a double-stranded RNA (dsRNA) but is not intended to be so limited and may comprise a single-stranded RNA (see, e.g., Martinez et al. Cell 110:563-74 (2002)). A siRNA polynucleotide may comprise other naturally occurring, recombinant, or synthetic single-stranded or double-stranded polymers of nucleotides (ribonucleotides or deoxyribonucleotides or a combination of both) and/or nucleotide analogues as provided herein (e.g., an oligonucleotide or polynucleotide or the like, typically in 5′ to 3′ phosphodiester linkage). Accordingly it will be appreciated that certain exemplary sequences disclosed herein as DNA sequences capable of directing the transcription of the subject invention siRNA polynucleotides are also intended to describe the corresponding RNA sequences and their complements, given the well established principles of complementary nucleotide base-pairing. A siRNA may be transcribed using as a template a DNA (genomic, cDNA, or synthetic) that contains a RNA polymerase promoter, for example, a U6 promoter or the H1 RNA polymerase III promoter, or the siRNA may be a synthetically derived RNA molecule. In certain embodiments the subject invention siRNA polynucleotide may have blunt ends, that is, each nucleotide in one strand of the duplex is perfectly complementary (e.g., by Watson-Crick base-pairing) with a nucleotide of the opposite strand. In certain other embodiments, at least one strand of the subject invention siRNA polynucleotide has at least one, and preferably two nucleotides that “overhang” (i.e., that do not base pair with a complementary base in the opposing strand) at the 3′ end of either strand, or preferably both strands, of the siRNA polynucleotide. In a preferred embodiment of the invention, each strand of the siRNA polynucleotide duplex has a two-nucleotide overhang at the 3′ end. The two-nucleotide overhang is preferably a thymidine dinucleotide (TT) but may also comprise other bases, for example, a TC dinucleotide or a TG dinucleotide, or any other dinucleotide. The overhang dinucleotide may also be complementary to the two nucleotides at the 5′ end of the sequence of the polynucleotide that is targeted for interference. For a discussion of 3′ ends of siRNA polynucleotides see, e.g., WO 01/75164.

[0078] Preferred siRNA polynucleotides comprise double-stranded oligomeric nucleotides of about 18-30 nucleotide base pairs, preferably about 18, 19, 20, 21, 22, 23, 24, 25, 26, or 27 base pairs, and in other preferred embodiments about 19, 20, 21, 22 or 23 base pairs, or about 27 base pairs, whereby the use of “about” indicates, as described above, that in certain embodiments and under certain conditions the processive cleavage steps that may give rise to functional siRNA polynucleotides that are capable of interfering with expression of a selected polypeptide may not be absolutely efficient. Hence, siRNA polynucleotides, for instance, of “about” 18, 19, 20, 21, 22, 23, 24, or 25 base pairs may include one or more siRNA polynucleotide molecules that may differ (e.g., by nucleotide insertion or deletion) in length by one, two, three or four base pairs, by way of non-limiting theory as a consequence of variability in processing, in biosynthesis, or in artificial synthesis. The contemplated siRNA polynucleotides of the present invention may also comprise a polynucleotide sequence that exhibits variability by differing (e.g., by nucleotide substitution, including transition or transversion) at one, two, three or four nucleotides from a particular sequence, the differences occurring at any of positions 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, or 19 of a particular siRNA polynucleotide sequence, or at positions 20, 21, 22, 23, 24, 25, 26, or 27 of siRNA polynucleotides depending on the length of the molecule, whether situated in a sense or in an antisense strand of the double-stranded polynucleotide. The nucleotide substitution may be found only in one strand, by way of example in the antisense strand, of a double-stranded polynucleotide, and the complementary nucleotide with which the substitute nucleotide would typically form hydrogen bond base pairing may not necessarily be correspondingly substituted in the sense strand. In preferred embodiments, the siRNA polynucleotides are homogeneous with respect to a specific nucleotide sequence. As described herein, preferred siRNA polynucleotides interfere with expression of a DSP-3, SHP-2, KAP, PRL-3, cdc14 or cdc25 polypeptide. These polynucleotides may also find uses as probes or primers.

[0079] Polynucleotides that are siRNA polynucleotides of the present invention may in certain embodiments be derived from a single-stranded polynucleotide that comprises a single-stranded oligonucleotide fragment (e.g., of about 18-30 nucleotides, which should be understood to include any whole integer of nucleotides including and between 18 and 30) and its reverse complement, typically separated by a spacer sequence. According to certain such embodiments, cleavage of the spacer provides the single-stranded oligonucleotide fragment and its reverse complement, such that they may anneal to form (optionally with additional processing steps that may result in addition or removal of one, two, three or more nucleotides from the 3′ end and/or the 5′ end of either or both strands) the double-stranded siRNA polynucleotide of the present invention. In certain embodiments the spacer is of a length that permits the fragment and its reverse complement to anneal and form a double-stranded structure (e.g., like a hairpin polynucleotide) prior to cleavage of the spacer (and, optionally, subsequent processing steps that may result in addition or removal of one, two, three, four, or more nucleotides from the 3′ end and/or the 5′ end of either or both strands). A spacer sequence may therefore be any polynucleotide sequence as provided herein that is situated between two complementary polynucleotide sequence regions which, when annealed into a double-stranded nucleic acid, comprise a siRNA polynucleotide. Preferably a spacer sequence comprises at least 4 nucleotides, although in certain embodiments the spacer may comprise 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, 21-25, 26-30, 31-40, 41-50, 51-70, 71-90, 91-110, 111-150, 151-200 or more nucleotides. Examples of siRNA polynucleotides derived from a single nucleotide strand comprising two complementary nucleotide sequences separated by a spacer have been described (e.g., Brummelkamp et al., 2002 Science 296:550; Paddison et al., 2002 Genes Develop. 16:948; Paul et al. Nat. Biotechnol. 20:505-508 (2002); Grabarek et al., BioTechniques 34:734-44 (2003)).

[0080] Polynucleotide variants may contain one or more substitutions, additions, deletions, and/or insertions such that the activity of the siRNA polynucleotide is not substantially diminished, as described above. The effect on the activity of the siRNA polynucleotide may generally be assessed as described herein, or using conventional methods. Variants preferably exhibit at least about 75%, 78%, 80%, 85%, 87%, 88% or 89% identity and more preferably at least about 90%, 92%, 95%, 96%, or 97% identity to a portion of a polynucleotide sequence that encodes a native DSP-3, SHP-2, KAP, PRL-3, cdc14 or cdc25. The percent identity may be readily determined by comparing sequences of the polynucleotides to the corresponding portion of the target polynucleotide, using any method including using computer algorithms well known to those having ordinary skill in the art, such as Align or the BLAST algorithm (Altschul, J. Mol. Biol. 219:555-565, 1991; Henikoff and Henikoff, Proc. Natl. Acad. Sci. USA 89:10915-10919, 1992), which is available at the NCBI website (see [online] Internet:<URL:http://www/ncbi.nlm.nih.gov/cgi-bin/BLAST). Default parameters may be used.

[0081] Certain siRNA polynucleotide variants are substantially homologous to a portion of a native gene that encodes a desired target polypeptide. Single-stranded nucleic acids derived (e.g., by thermal denaturation) from such polynucleotide variants are capable of hybridizing under moderately stringent conditions to a naturally occurring DNA or RNA sequence encoding a native target polypeptide. In a preferred embodiment of the invention, a siRNA polynucleotide that detectably hybridizes under moderately stringent conditions to a target polypeptide-encoding polynucleotide comprises a nucleotide sequence other than SEQ ID NO:10, which is disclosed in Mailand et al. (2002 Nature Cell Biol. 4:317). A siRNA polynucleotide that detectably hybridizes under moderately stringent conditions may have a nucleotide sequence that includes at least 10 consecutive nucleotides, more preferably 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, 21, 22, 23, 24, 25, 26, 27, 28, 29 or 30 consecutive nucleotides that are complementary to a particular target polynucleotide. In certain preferred embodiments such a siRNA sequence (or its complement) will be unique to a single particular target polypeptide for which interference with expression is desired, and in certain other embodiments the sequence (or its complement) may be shared by two or more related target polypeptides for which interference with polypeptide expression is desired.

[0082] Suitable moderately stringent conditions include, for example, pre-washing in a solution of 5×SSC, 0.5% SDS, 1.0 mM EDTA (pH 8.0); hybridizing at 50° C.-70° C., 5×SSC for 1-16 hours (e.g., overnight); followed by washing once or twice at 22-65° C. for 20-40 minutes with one or more each of 2×, 0.5× and 0.2×SSC containing 0.05-0.1% SDS. For additional stringency, conditions may include a wash in 0.1×SSC and 0.1% SDS at 50-60° C. for 15-40 minutes. As known to those having ordinary skill in the art, variations in stringency of hybridization conditions may be achieved by altering the time, temperature, and/or concentration of the solutions used for pre-hybridization, hybridization, and wash steps. Suitable conditions may also depend in part on the particular nucleotide sequences of the probe used, and of the blotted, proband nucleic acid sample. Accordingly, it will be appreciated that suitably stringent conditions can be readily selected without undue experimentation when a desired selectivity of the probe is identified, based on its ability to hybridize to one or more certain proband sequences while not hybridizing to certain other proband sequences.

[0083] Sequence specific siRNA polynucleotides of the present invention may be designed using one or more of several criteria. For example, to design a siRNA polynucleotide that has 19 consecutive nucleotides identical to a sequence encoding a polypeptide of interest (e.g., PTP1B and other polypeptides described herein), the open reading frame of the polynucleotide sequence may be scanned for 21-base sequences that have one or more of the following characteristics: (1) an A+T/G+C ratio of approximately 1:1 but no greater than 2:1 or 1:2; (2) an AA dinucleotide or a CA dinucleotide at the 5′ end; (3) an internal hairpin loop melting temperature less than 55° C.; (4) a homodimer melting temperature of less than 37° C. (melting temperature calculations as described in (3) and (4) can be determined using computer software known to those skilled in the art); (5) a sequence of at least 16 consecutive nucleotides not identified as being present in any other known polynucleotide sequence (such an evaluation can be readily determined using computer programs available to a skilled artisan such as BLAST to search publicly available databases). Alternatively, a siRNA polynculeotide sequence may be designed and chosen using a computer software available commercially from various vendors (e.g., OligoEngine™ (Seattle, Wash.); Dharmacon, Inc. (Lafayette, Colo.); Ambion Inc. (Austin, Tex.); and QIAGEN, Inc. (Valencia, Calif.)). (See also Elbashir et al., Genes & Development 15:188-200 (2000); Elbashir et al., Nature 411:494-98 (2001); and [online] Internet:URL<http://www.mpibpc.gwdg.de/abteilungen/100/105/Tusch1_MIV2(3) 2002.pdf.) The siRNA polynucleotides may then be tested for their ability to interfere with the expression of the target polypeptide according to methods known in the art and described herein. The determination of the effectiveness of an siRNA polynucleotide includes not only consideration of its ability to interfere with polypeptide expression but also includes consideration of whether the siRNA polynucleotide manifests undesirably toxic effects, for example, apoptosis of a cell for which cell death is not a desired effect of RNA interference (e.g., interference of PTP1B expression in a cell).

[0084] It should be appreciated that not all siRNAs designed using the above methods will be effective at silencing or interfering with expression of a desired target polypeptide. And further, that the siRNAs will effect silencing to different degrees. Such siRNAs must be tested for their effectiveness, and selections made therefrom based on the ability of a given siRNA to interfere with or modulate (e.g., decrease in a statistically significant manner) the expression of the target. Accordingly, identification of specific siRNA polynucleotide sequences that are capable of interfering with expression of a desired target polypeptide requires production and testing of each siRNA, as demonstrated in greater detail below (see Examples).

[0085] Furthermore, not all siRNAs that interfere with protein expression will have a physiologically important effect. The inventors here have designed, and describe herein, physiologically relevant assays for measuring the influence of modulated target polypeptide expression, for instance, cellular proliferation, induction of apoptosis, and/or altered levels of protein tyrosine phosphorylation (e.g., insulin receptor phosphorylation), to determine if the levels of interference with target protein expression that were observed using the siRNAs of the invention have clinically relevant significance. Additionally, and according to non-limiting theory, the invention contemplates altered (e.g., decreased or increased in a statistically significant manner) expression levels of one or more polypeptides of interest, and/or altered (i.e., increased or decreased) phosphorylation levels of one or more phosphoproteins of interest, which altered levels may result from impairment of target protein expression and/or cellular compensatory mechanisms that are induced in response to RNAi-mediated inhibition of a specific target polypeptide expression.

[0086] Persons having ordinary skill in the art will also readily appreciate that as a result of the degeneracy of the genetic code, many nucleotide sequences may encode a polypeptide as described herein. That is, an amino acid may be encoded by one of several different codons and a person skilled in the art can readily determine that while one particular nucleotide sequence may differ from another (which may be determined by alignment methods disclosed herein and known in the art), the sequences may encode polypeptides with identical amino acid sequences. By way of example, the amino acid leucine in a polypeptide may be encoded by one of six different codons (TTA, TTG, CTT, CTC, CTA, and CTG) as can serine (TCT, TCC, TCA, TCG, AGT, and AGC). Other amino acids, such as proline, alanine, and valine, for example, may be encoded by any one of four different codons (CCT, CCC, CCA, CCG for proline; GCT, GCC, GCA, GCG for alanine; and GTT, GTC, GTA, GTG for valine). Some of these polynucleotides bear minimal homology to the nucleotide sequence of any native gene. Nonetheless, polynucleotides that vary due to differences in codon usage are specifically contemplated by the present invention.

[0087] Polynucleotides, including target polynucleotides, may be prepared using any of a variety of techniques, which will be useful for the preparation of specifically desired siRNA polynucleotides and for the identification and selection of desirable sequences to be used in siRNA polynucleotides. For example, a polynucleotide may be amplified from cDNA prepared from a suitable cell or tissue type. Such polynucleotides may be amplified via polymerase chain reaction (PCR). For this approach, sequence-specific primers may be designed based on the sequences provided herein and may be purchased or synthesized. An amplified portion may be used to isolate a full-length gene, or a desired portion thereof, from a suitable library (e.g., human skeletal muscle cDNA) using well known techniques. Within such techniques, a library (cDNA or genomic) is screened using one or more polynucleotide probes or primers suitable for amplification. Preferably, a library is size-selected to include larger molecules. Random primed libraries may also be preferred for identifying 5′ and upstream regions of genes. Genomic libraries are preferred for obtaining introns and extending 5′ sequences. Suitable sequences for a siRNA polynucleotide contemplated by the present invention may also be selected from a library of siRNA polynucleotide sequences.

[0088] For hybridization techniques, a partial sequence may be labeled (e.g., by nick-translation or end-labeling with ³²P) using well known techniques. A bacterial or bacteriophage library may then be screened by hybridizing filters containing denatured bacterial colonies (or lawns containing phage plaques) with the labeled probe (see, e.g., Sambrook et al., Molecular Cloning: A Laboratory Manual, Cold Spring Harbor Laboratories, Cold Spring Harbor, N.Y., 2001). Hybridizing colonies or plaques are selected and expanded, and the DNA is isolated for further analysis. Clones may be analyzed to determine the amount of additional sequence by, for example, PCR using a primer from the partial sequence and a primer from the vector. Restriction maps and partial sequences may be generated to identify one or more overlapping clones. A full-length cDNA molecule can be generated by ligating suitable fragments, using well known techniques.

[0089] Alternatively, numerous amplification techniques are known in the art for obtaining a full-length coding sequence from a partial cDNA sequence. Within such techniques, amplification is generally performed via PCR. One such technique is known as “rapid amplification of cDNA ends” or RACE. This technique involves the use of an internal primer and an external primer, which hybridizes to a polyA region or vector sequence, to identify sequences that are 5′ and 3′ of a known sequence. Any of a variety of commercially available kits may be used to perform the amplification step. Primers may be designed using, for example, software well known in the art. Primers (or oligonucleotides for other uses contemplated herein, including, for example, probes and antisense oligonucleotides) are preferably 15, 16, 17, 18, 19, 20, 21, 22, 23, 24, 25, 26, 27, 28, 29, 30, 31 or 32 nucleotides in length, have a GC content of at least 40% and anneal to the target sequence at temperatures of about 54° C. to 72° C. The amplified region may be sequenced as described above, and overlapping sequences assembled into a contiguous sequence. Certain oligonucleotides contemplated by the present invention may, for some preferred embodiments, have lengths of 18, 19, 20, 21, 22, 23, 24, 25, 26, 27, 28, 29, 30, 31, 32, 33-35, 35-40, 41-45, 46-50, 56-60, 61-70, 71-80, 81-90 or more nucleotides.

[0090] A number of specific siRNA polynucleotide sequences useful for interfering with target polypeptide expression, and are presented in the Examples, the Drawings, and the Sequence Listing. SiRNA polynucleotides may generally be prepared by any method known in the art, including, for example, solid phase chemical synthesis. Modifications in a polynucleotide sequence may also be introduced using standard mutagenesis techniques, such as oligonucleotide-directed site-specific mutagenesis. Further, siRNAs may be chemically modified or conjugated to improve theur serum stability and/or delivery properties. Included as an aspect of the invention are the siRNAs described herein wherein the ribose has been removed therefrom. Alternatively, siRNA polynucleotide molecules may be generated by in vitro or in vivo transcription of suitable DNA sequences (e.g., polynucleotide sequences encoding a target polypeptide, or a desired portion thereof), provided that the DNA is incorporated into a vector with a suitable RNA polymerase promoter (such as T7, U6, H1, or SP6). In addition, a siRNA polynucleotide may be administered to a patient, as may be a DNA sequence (e.g., a recombinant nucleic acid construct as provided herein) that supports transcription (and optionally appropriate processing steps) such that a desired siRNA is generated in vivo.

[0091] Accordingly, a siRNA polynucleotide that is complementary to at least a portion of a target polypeptide-encoding sequence may be used to modulate gene expression, or as a probe or primer. Identification of siRNA polynucleotide sequences and DNA encoding genes for their targeted delivery involves techniques described herein. Identification of such siRNA polynucleotide sequences and DNA encoding genes for their targeted delivery involves techniques that are also described herein. As discussed above, siRNA polynucleotides exhibit desirable stability characteristics and may, but need not, be further designed to resist degradation by endogenous nucleolytic enzymes by using such linkages as phosphorothioate, methylphosphonate, sulfone, sulfate, ketyl, phosphorodithioate, phosphoramidate, phosphate esters, and other such linkages (see, e.g., Agrwal et al., Tetrahedron Lett. 28:3539-3542 (1987); Miller et al., J. Am. Chem. Soc. 93:6657-6665 (1971); Stec et al., Tetrahedron Lett. 26:2191-2194 (1985); Moody et al., Nucleic Acids Res. 12:4769-4782 (1989); Uznanski et al., Nucleic Acids Res. (1989); Letsinger et al., Tetrahedron 40:137-143 (1984); Eckstein, Annu. Rev. Biochem. 54:367402 (1985); Eckstein, Trends Biol. Sci. 14:97-100 (1989); Stein, In: Oligodeoxynucleotides. Antisense Inhibitors of Gene Expression, Cohen, ed., Macmillan Press, London, pp. 97-117 (1989); Jager et al., Biochemistry 27:7237-7246 (1988)).

[0092] Any polynucleotide of the invention may be further modified to increase stability in vivo. Possible modifications include, but are not limited to, the addition of flanking sequences at the 5′ and/or 3′ ends; the use of phosphorothioate or 2′ O-methyl rather than phosphodiester linkages in the backbone; and/or the inclusion of nontraditional bases such as inosine, queosine, and wybutosine and the like, as well as acetyl- methyl-, thio- and other modified forms of adenine, cytidine, guanine, thymine, and uridine.

[0093] Nucleotide sequences as described herein may be joined to a variety of other nucleotide sequences using established recombinant DNA techniques. For example, a polynucleotide may be cloned into any of a variety of cloning vectors, including plasmids, phagemids, lambda phage derivatives, and cosmids. Vectors of particular interest include expression vectors, replication vectors, probe generation vectors, and sequencing vectors. In general, a suitable vector contains an origin of replication functional in at least one organism, convenient restriction endonuclease sites, and one or more selectable markers. (See, e.g., WO 01/96584; WO 01/29058; U.S. Pat. No. 6,326,193; U.S. 2002/0007051). Other elements will depend upon the desired use, and will be apparent to those having ordinary skill in the art. For example, the invention contemplates the use of siRNA polynucleotide sequences in the preparation of recombinant nucleic acid constructs including vectors for interfering with the expression of a desired target polypeptide such as a PTP polypeptide, a MAP kinase kinase polypeptide, or a chemotherapeutic target polypeptide in vivo; the invention also contemplates the generation of siRNA transgenic or “knock-out” animals and cells (e.g., cells, cell clones, lines or lineages, or organisms in which expression of one or more desired polypeptides (e.g., a target polypeptide) is fully or partially compromised). An siRNA polynucleotide that is capable of interfering with expression of a desired polypeptide (e.g., a target polypeptide) as provided herein thus includes any siRNA polynucleotide that, when contacted with a subject or biological source as provided herein under conditions and for a time sufficient for target polypeptide expression to take place in the absence of the siRNA polynucleotide, results in a statistically significant decrease (alternatively referred to as “knockdown” of expression) in the level of target polypeptide expression that can be detected. Preferably the decrease is greater than 10%, more preferably greater than 20%, more preferably greater than 30%, more preferably greater than 40%, 50%, 60%, 70%, 75%, 80%, 85%, 90%, 95% or 98% relative to the expression level of the polypeptide detected in the absence of the siRNA, using conventional methods for determining polypeptide expression as known to the art and provided herein. Preferably, the presence of the siRNA polynucleotide in a cell does not result in or cause any undesired toxic effects, for example, apoptosis or death of a cell in which apoptosis is not a desired effect of RNA interference.

[0094] Within certain embodiments, siRNA polynucleotides may be formulated so as to permit entry into a cell of a mammal, and expression therein. Such formulations are particularly useful for therapeutic purposes, as described below. Those having ordinary skill in the art will appreciate that there are many ways to achieve expression of a polynucleotide in a target cell, and any suitable method may be employed. For example, a polynucleotide may be incorporated into a viral vector using well known techniques (see also, e.g., U.S. 2003/0068821). A viral vector may additionally transfer or incorporate a gene for a selectable marker (to aid in the identification or selection of transduced cells) and/or a targeting moiety, such as a gene that encodes a ligand for a receptor on a specific target cell, to render the vector target specific. Targeting may also be accomplished using an antibody, by methods known to those having ordinary skill in the art.

[0095] Other formulations for therapeutic purposes include colloidal dispersion systems, such as macromolecule complexes, nanocapsules, microspheres, beads, and lipid-based systems including oil-in-water emulsions, micelles, mixed micelles, and liposomes. A preferred colloidal system for use as a delivery vehicle in vitro and in vivo is a liposome (i.e., an artificial membrane vesicle). The preparation and use of such systems is well known in the art.

[0096] Within other embodiments, one or more promoters may be identified, isolated and/or incorporated into recombinant nucleic acid constructs of the present invention, using standard techniques. The present invention provides nucleic acid molecules comprising such a promoter sequence or one or more cis- or trans-acting regulatory elements thereof. Such regulatory elements may enhance or suppress expression of a siRNA. A 5′ flanking region may be generated using standard techniques, based on the genomic sequence provided herein. If necessary, additional 5′ sequences may be generated using PCR-based or other standard methods. The 5′ region may be subcloned and sequenced using standard methods. Primer extension and/or RNase protection analyses may be used to verify the transcriptional start site deduced from the cDNA.

[0097] To define the boundary of the promoter region, putative promoter inserts of varying sizes may be subcloned into a heterologous expression system containing a suitable reporter gene without a promoter or enhancer. Suitable reporter genes may include genes encoding luciferase, beta-galactosidase, chloramphenicol acetyl transferase, secreted alkaline phosphatase, or the Green Fluorescent Protein gene (see, e.g., Ui-Tei et al., FEBS Lett. 479:79-82 (2000). Suitable expression systems are well known and may be prepared using well known techniques or obtained commercially. Internal deletion constructs may be generated using unique internal restriction sites or by partial digestion of non-unique restriction sites. Constructs may then be transfected into cells that display high levels of siRNA polynucleotide and/or polypeptide expression. In general, the construct with the minimal 5′ flanking region showing the highest level of expression of reporter gene is identified as the promoter. Such promoter regions may be linked to a reporter gene and used to evaluate agents for the ability to modulate promoter-driven transcription.

[0098] Once a functional promoter is identified, cis- and trans-acting elements may be located. Cis-acting sequences may generally be identified based on homology to previously characterized transcriptional motifs. Point mutations may then be generated within the identified sequences to evaluate the regulatory role of such sequences. Such mutations may be generated using site-specific mutagenesis techniques or a PCR-based strategy. The altered promoter is then cloned into a reporter gene expression vector, as described above, and the effect of the mutation on reporter gene expression is evaluated.

[0099] In general, polypeptides and polynucleotides as described herein are isolated. An “isolated” polypeptide or polynucleotide is one that is removed from its original environment. For example, a naturally occurring protein is isolated if it is separated from some or all of the coexisting materials in the natural system. Preferably, such polypeptides are at least about 90% pure, more preferably at least about 95% pure and most preferably at least about 99% pure. A polynucleotide is considered to be isolated if, for example, it is cloned into a vector that is not a part of the natural environment. A “gene” includes the segment of DNA involved in producing a polypeptide chain; it further includes regions preceding and following the coding region “leader and trailer,” for example promoter and/or enhancer and/or other regulatory sequences and the like, as well as intervening sequences (introns) between individual coding segments (exons).

[0100] As noted above, according to certain embodiments of the invention compositions and methods are provided that relate to altering or altered expression of a PTP as described herein (including DSPs) or of other target polypeptides as disclosed herein, and/or to a PTP associated disorder. A PTP associated disorder includes any disease, disorder, condition, syndrome, pathologic or physiologic state, or the like, wherein at least one undesirable deviation or departure from a physiological norm causes, correlates with, is accompanied by or results from an inappropriate alteration (i.e., a statistically significant change) to the structure, activity, function, expression level, physicochemical or hydrodynamic property, or stability of a PTP or of a molecular component of a biological signal transduction pathway that comprises a PTP, for instance, a MAP kinase such as JNK (e.g., Shen et al., 2001 Proc. Nat. Acad. Sci. USA 98:13613; see also U.S. Pat. No. 6,342,595), TYK2 or Jak2 (e.g., Myers et al., 2001.J. Biol. Chem. 276:47771), or a MAP kinase kinase MKK4 or MKK7 (e.g., Shen et al., Proc. Natl. Acad. Sci. USA 98:13613-18 (2001) and references cited therein), a receptor such as IR (Salmeen et al., 2000), or leptin receptor (e.g., Kalman et al. 2000 and references cited therein) or other such pathways comprising PTPs as known to the art. In preferred embodiments the molecular component may be a protein, peptide or polypeptide, and in certain other preferred embodiments the alteration may be an altered level of PTP expression. In certain other preferred embodiments the alteration may be manifest as an a typical or unusual phosphorylation state of a protein under particular conditions, for example, hypophosphorylation or hyperphosphorylation of a phosphoprotein, wherein those familiar with the art will appreciate that phosphorylated proteins typically comprise one or more phosphotyrosine, phosphoserine, or phosphothreonine residues.

[0101] PTP associated disorders therefore include, for example, diabetes mellitus, obesity, impaired glucose tolerance and other metabolic disorders wherein alteration of a biological signaling pathway component is associated with the disorder The effect of siRNA interference with expression of a component in the signal transduction pathway induced by insulin, for example, may be evaluated by determining the level of tyrosine phosphorylation of insulin receptor beta (IR-β) and/or of the downstream signaling molecule PKB/Akt and/or of any other downstream polypeptide that may be a component of a particular signal transduction pathway as provided herein. The invention is not intended, however, to be so limited and contemplates other disorders, such as JNK-associated disorders (e.g., cancer, cardiac hypertrophy, ischemia, diabetes, hyperglycemia-induced apoptosis, inflammation, neurodegenerative disorders), and other disorders associated with different signal transduction pathways, for instance, cancer, autoimmunity, cellular proliferative disorders, neurodegenerative disorders, and infectious diseases (see, e.g., Fukada et al., 2001 J. Biol. Chem. 276:25512; Tonks et al., 2001 Curr. Opin. Cell Biol. 13:182; Salmeen et al., 2000 Mol. Cell 6:1401; Hu et al., J. Neurochem. 85:432-42 (2003); and references cited therein).

[0102] Cancer is also associated with other dual specificity phosphatases, such as DSP-3, PRL-3 (see, e.g., Saha et al., Science 294:1343-46 (2001), PTPε (Elson, Oncogene 18:7535-42 (1999)), and the cell cycle dual specificity phosphatases cdc25 (see, e.g., Donzelli et al., EMBO 21:4875-84 (2002), cdc14 (Wong et al., Genomics 59:248-51 (1999)), and KAP (see, e.g., Lee et al., Mol. Cell Biol. 20:1723-32 (2000); Yeh et al., Cancer Res. 60:4697-700 (2000); see also, e.g., Donato et al., J. Clin. Invest. 109:51-58 (2002)). Another dual specificity phosphatase believed to be involved in the cell cycle, cdc14, is reported to interact with the tumor suppressor protein p53 (Li et al., J. Biol. Chem. 275:2410014 (2000); see also Agami et al., Cell 102:55-66 (2000)). In normal cells, cdc14 is reported to be a part of the mitotic exit network, which involves intricate regulatory pathways that coordinate chromosome segregation and mitotic exit with physical separation of two nascent cells, and in cytokineses (see, e.g., Gruneberg et al., J. Cell Biol. 158:901-14 (2002); Trautman et al., Curr. Biol. 12:R733-R735 (2002); Visintin et al., Mol. Cell 2:709-18 (1998); see also Mailand et al., supra). Persons skilled in the art will be familiar with an array of criteria according to which it may be recognized what are, for instance, biological, physiological, pathological and/or clinical signs and/or symptoms of PTP associated and other disorders as provided herein (see, e.g., Irie-Sasaki et al., Curr. Top. Med. Chem. 3:783-96 (2003) (discussing role of CD45 in signal transduction pathways); Oh et al., Mol. Cell Biol. 19:3205-15 (1999) (describing regulation of early events in integrin signaling by SHP-2); Musante et al., Eur. J. Hum. Genet. 11:201-206 (2003), Tartaglia et al., Nat. Genet. 29:465-68 (2001), and Ion et al., Hum. Genet. 111:421-27 (2002) (discussing correlation between mutations in the PTPN11 gene that encodes SHP-2 and Noonan Syndrome)); Tanuma et al., Blood 98:3030-34 (2001) (reporting that PTPε inhibits IL-6 and IL-10 induced JAK-STAT signaling)).

[0103] Also contemplated by the invention are disorders associated with the NF-kappaB signaling pathway, for example, in cancer cells in which NF-kappaB is overexpressed or constitutively activated (see, e.g., Bayon et al., Mol. Cell Biol. 23:1061-74 (2003); Arsura et al., Oncogene 22:412-25 (2003)). Other disorders associated with the NF-kappaB signaling pathway include those associated with other components of the pathway, for example, inflammation associated with IkappaB kinase gamma (IKKgamma), which is an upstream regulator of NF-kappaB that is required for NF-kappaB activation by various stimuli (see, e.g., Makris et al., Mol. Cell Biol. 22:6573-81 (2002); Li et al., J. Biol. Chem. 277:45129-40 (2002); Sadikot et al., J. Immunol. 170:1091-98 (2003)).

[0104] As noted above, regulated tyrosine phosphorylation contributes to specific pathways for biological signal transduction, including those associated with cell division, cell survival, apoptosis, proliferation and differentiation, and “biological signal transduction pathways,” or “inducible signaling pathways” in the context of the present invention include transient or stable associations or interactions among molecular components involved in the control of these and similar processes in cells. Depending on the particular pathway of interest, an appropriate parameter for determining induction of such pathway may be selected. For example, for signaling pathways associated with cell proliferation, a variety of well known methodologies are available for quantifying proliferation, including, for example, incorporation of tritiated thymidine into cellular DNA, monitoring of detectable (e.g., fluorimetric or calorimetric) indicators of cellular respiratory activity (for example, conversion of the tetrazolium salts (yellow) 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT) or 3-(4,5-dimethylthiazol-2-yl)-5-(3-carboxymethoxyphenyl)-2-(4-sulphophenyl)-2H-tetrazolium (MTS) to formazan dyes (purple) in metabolically active cells), or cell counting, or the like. Similarly, in the cell biology arts, multiple techniques are known for assessing cell survival (e.g., vital dyes, metabolic indicators, etc.) and for determining apoptosis (for example, annexin V binding, DNA fragmentation assays, caspase activation, marker analysis, e.g., poly(ADP-ribose) polymerase (PARP), etc.). Other signaling pathways will be associated with particular cellular phenotypes, for example specific induction of gene expression (e.g., detectable as transcription or translation products, or by bioassays of such products, or as nuclear localization of cytoplasmic factors), altered (e.g., statistically significant increases or decreases) levels of intracellular mediators (e.g., activated kinases or phosphatases, altered levels of cyclic nucleotides or of physiologically active ionic species, etc.), altered cell cycle profiles, or altered cellular morphology, and the like, such that cellular responsiveness to a particular stimulus as provided herein can be readily identified to determine whether a particular cell comprises an inducible signaling pathway.

[0105] In addition, according to certain embodiments of the invention compositions and methods are provided that relate to altering or altered expression of chemotherapeutic target polypeptides. Sequence specific siRNA polynucleotides may be used as a conjunctive therapy with chemotherapeutic drugs or may provide an alternative therapy in circumstances when a cancer becomes refractory to chemotherapeutic treatment regimens. Resistance to chemotherapeutic drugs may develop when a chemotherapeutic target polypeptide is overexpressed or when its expression becomes constitutive. Overexpression or amplified expression of such a target polypeptide could be reduced by introducing a specific siRNA polynucleotide into the cell. In particular, chemotherapeutic target polypeptides that may become resistant to drug therapies include, for example, components of the thymidylate biosynthesis pathway, thymidylate synthetase and DHFR, which become refractory to anti-neoplastic drugs such as 5-FU and methotrexate, respectively, and contribute to a drug resistance phenotype. Also contemplated by the invention are sequence specific siRNA polynucleotides that interfere with expression of DNA-processing enzymes such as topoisomerase I and that would have anti-cancer or anti-bacterial effects. The effect of siRNA interference on expression of such chemotherapeutic target polypeptides may alter cell division, cell survival, apoptosis, proliferation, and differentiation, which may be assessed by any of the techniques and methods described herein.

[0106] PTPs

[0107] As used herein, a phosphatase is a member of the PTP family if it contains the signature motif CX₅R (SEQ ID NO:______). Dual specificity PTPs, i.e., PTPs that dephosphorylate both phosphorylated tyrosine and phosphorylated serine or threonine, are also suitable for use in the invention. PTPs for use in the present invention include PTP1B (e.g., GenBank Accession Nos. M31724 (SEQ ID NOS: ______-______); NM_(—)002827 (SEQ ID NOS: ______-______); NM_(—)011201 (SEQ ID NOS: ______-______); M31724 (SEQ ID NOS: ______-______); M33689 (SEQ ID NOS: ______-______); M33962 (SEQ ID NOS: ______-______)). In certain preferred embodiments, TC-PTP (e.g., GenBank Accession Nos. M25393 (SEQ ID NOS: ______-______); M81478 (SEQ ID NO: ______); M80737 (SEQ ID NO: ______); M81477 (SEQ ID NOS: ______-______); X58828 (SEQ ID NOS: ______-______); NM_(—)002828 (SEQ ID NOS: ______ and ______)) and TC45 (e.g., NM_(—)080422 (SEQ ID NOS: ______ and ______)) may be used. In certain other embodiments PTPs and DSPs for use in the present invention include DSP-3 (WO00/60092); SHP2, (e.g., GenBank Accession Nos. D13540 (SEQ ID NOS: ______-______); L03535 (SEQ ID NOS: ______-______); L07527 (SEQ ID NOS: ______-______); X70766 (SEQ ID NOS: ______-______); L08807 (SEQ ID NO: ______); S78088 (SEQ ID NOS: ______-______); S39383 (SEQ ID NO: ______); D84372 (SEQ ID NOS: ______-______); U09307 (SEQ ID NOS: 15-16)); cdc14 (which includes cdc14a (e.g., GenBank Accession Nos. AF122013 (SEQ ID NOS: ______-______); AF064102 (SEQ ID NOS: ______-______); AF064103 (SEQ ID NOS: ______-______); Li et al., 1997 J. Biol. Chem. 272:29403; U.S. Pat. No. 6,331,614) and cdc14b (e.g., GenBank Accession Nos. AF064104 (SEQ ID NOS: ______-______); AF064105 (SEQ ID NOS: ______-______); CDC25A ((e.g., GenBank Accession Nos. NM_(—)001789 (SEQ ID NOS: ______-______), AF527417 (SEQ ID NOS: ______-______), NM_(—)133571 (SEQ ID NOS: ______-______)); CDC25B (e.g., GenBank Accession Nos. NM_(—)133572 (SEQ ID NOS: ______-______), NM_(—)023117 (SEQ ID NOS: ______-______), NM_(—)021872 (SEQ ID NOS: ______-______); NM_(—)021872; M81934) (SEQ ID NOS: ______-______); and CDC25C (e.g., GenBank Accession Nos. NM_(—)001790 (SEQ ID NOS: ______-______), NM_(—)022809 (SEQ ID NOS: ______-______)); CD45 (Charbonneau et al., Proc. Natl. Acad. Sci. USA 85:7182-86 (1988); Genbank Accession Nos. NM_(—)080922 (SEQ ID NOS: ______-______), NM_(—)080921 (SEQ ID NOS: ______-______), NM_(—)002838 (SEQ ID NOS: ______-______), and NM_(—)080923) (SEQ ID NOS: ______-______); GenBank Acc. No. XM_(—)16748; SEQ ID NO:32 encoded by SEQ ID NO:31; KAP (Genbank Accession No. L27711 (SEQ ID NOS: ______-______); Hannon et al., Proc. Natl. Acad. Sci. USA 91:1731-35 (1994)); PTPε (e.g., Genbank Accession Nos. NM_(—)006504 (SEQ ID NOS: ______-______) and NM_(—)130435 (SEQ ID NOS: ______-______)); and PRL-3 (e.g., Zhao et al., Genomics 35:172-81 (1996); Genbank Accession Nos. (NM 003479 (SEQ ID NOS: ______-______), NM_(—)080392 (SEQ ID NOS: ______-______), NM_(—)080391 (SEQ ID NOS: ______-______), NM_(—)032611 (SEQ ID NOS: ______-______), and NM_(—)007079 (SEQ ID NOS: ______-______). In certain preferred embodiments PTPs and DSPs include, but are not limited to, U.S. application Ser. No. 10/151,320 (DSP18); WO 01/05983 (DSP-11); U.S. application Ser. No. 09/775,925 (DSP-12 and DSP-13); U.S. application Ser. No. 09/847,519 and WO 01/46394 (DSP-14); The invention also contemplates using mutated forms of the PTPs and DSPs, which may include PTPs and DSPs that contain single nucleotide polymorphisms (SNPs), or may include allelic forms.

[0108] Specific substitutions of individual amino acids through introduction of site-directed mutations are well-known and may be made according to methodologies with which those having ordinary skill in the art will be familiar. The effects on catalytic activity of the resulting mutant PTP may be determined empirically by testing the resulting modified protein for the preservation of the Km and reduction of Kcat to less than 1 per minute as provided herein and as previously disclosed (e.g., WO98/04712; Flint et al., 1997 Proc. Nat. Acad. Sci. USA 94:1680). In addition, the effect on phosphorylatation of one or more tyrosine residues of the resulting mutant PTP molecule can also be determined empirically merely by testing such a mutant for the presence of phosphotyrosine, as also provided herein, for example, following exposure of the mutant to conditions in vitro or in vivo where it may act as a phosphate acceptor for a protein tyrosine kinase.

[0109] In particular, portions of two PTP polypeptide sequences are regarded as “corresponding” amino acid sequences, regions, fragments or the like, based on a convention of numbering one PTP sequence according to amino acid position number, and then aligning the sequence to be compared in a manner that maximizes the number of amino acids that match or that are conserved residues, for example, that remain polar (e.g., D, E, K, R, H, S, T, N, Q), hydrophobic (e.g., A, P, V, L, I, M, F, W, Y) or neutral (e.g., C, G) residues at each position. Similarly, a DNA sequence encoding a candidate PTP that is to be mutated as provided herein, or a portion, region, fragment or the like, may correspond to a known wildtype PTP-encoding DNA sequence according to a convention for numbering nucleic acid sequence positions in the known wildtype PTP DNA sequence, whereby the candidate PTP DNA sequence is aligned with the known PTP DNA such that at least 70%, preferably at least 80% and more preferably at least 90% of the nucleotides in a given sequence of at least 20 consecutive nucleotides of a sequence are identical. In certain preferred embodiments, a candidate PTP DNA sequence is greater than 95% identical to a corresponding known PTP DNA sequence. In certain particularly preferred embodiments, a portion, region or fragment of a candidate PTP DNA sequence is identical to a corresponding known PTP DNA sequence. As is well known in the art, an individual whose DNA contains no irregularities (e.g., a common or prevalent form) in a particular gene responsible for a given trait may be said to possess a wildtype genetic complement (genotype) for that gene, while the presence of irregularities known as mutations in the DNA for the gene, for example, substitutions, insertions or deletions of one or more nucleotides, indicates a mutated or mutant genotype. The invention need not be so limited, however, and contemplates other embodiments wherein two or more non-PTP polypeptides of interest (e.g., as siRNA targets), such as MAP kinase kinases or chemotherapeutic target polypeptides, are structurally related and have portions of polypeptide sequences that may be regarded as “corresponding” amino acid sequences, regions, fragments or the like, according to the alignment and identity criteria discussed above.

[0110] Modification of DNA may be performed by a variety of methods, including site-specific or site-directed mutagenesis of DNA encoding the polypeptide of interest (e.g., a siRNA target polypeptide) and the use of DNA amplification methods using primers to introduce and amplify alterations in the DNA template, such as PCR splicing by overlap extension (SOE). Site-directed mutagenesis is typically effected using a phage vector that has single- and double-stranded forms, such as M13 phage vectors, which are well-known and commercially available. Other suitable vectors that contain a single-stranded phage origin of replication may be used (see, e.g., Veira et al., Meth. Enzymol. 15:3, 1987). In general, site-directed mutagenesis is performed by preparing a single-stranded vector that encodes the protein of interest (e.g., a member of the PTP family, a MAP kinase kinase, or a chemotherapeutic target polypeptide). An oligonucleotide primer that contains the desired mutation within a region of homology to the DNA in the single-stranded vector is annealed to the vector followed by addition of a DNA polymerase, such as E. coli DNA polymerase I (Klenow fragment), which uses the double stranded region as a primer to produce a heteroduplex in which one strand encodes the altered sequence and the other the original sequence. Additional disclosure relating to site-directed mutagenesis may be found, for example, in Kunkel et al. (Methods in Enzymol. 154:367, 1987) and in U.S. Pat. Nos. 4,518,584 and 4,737,462. The heteroduplex is introduced into appropriate bacterial cells, and clones that include the desired mutation are selected. The resulting altered DNA molecules may be expressed recombinantly in appropriate host cells to produce the modified protein.

[0111] SiRNAs of the invention may be fused to other nucleotide molecules, or to polypeptides, in order to direct their delivery or to accomplish other functions. Thus, for example, fusion proteins comprising a siRNA oligonucleotide that is capable of specifically interfering with expression of a target polypeptide may comprise affinity tag polypeptide sequences, which refers to polypeptides or peptides that facilitate detection and isolation of the such polypeptide via a specific affinity interaction with a ligand. The ligand may be any molecule, receptor, counterreceptor, antibody or the like with which the affinity tag may interact through a specific binding interaction as provided herein. Such peptides include, for example, poly-His or “FLAG®” or the like, e.g., the antigenic identification peptides described in U.S. Pat. No. 5,011,912 and in Hopp et al., (1988 Bio/Technology 6:1204), or the XPRESS™ epitope tag (Invitrogen, Carlsbad, Calif.). The affinity sequence may be a hexa-histidine tag as supplied, for example, by a pBAD/His (Invitrogen) or a pQE-9 vector to provide for purification of the mature polypeptide fused to the marker in the case of a bacterial host, or, for example, the affinity sequence may be a hemagglutinin (HA) tag when a mammalian host, e.g., COS-7 cells, is used. The HA tag corresponds to an antibody defined epitope derived from the influenza hemagglutinin protein (Wilson et al., 1984 Cell 37:767).

[0112] The present invention also relates to vectors and to constructs that include or encode siRNA polynucleotides of the present invention, and in particular to “recombinant nucleic acid constructs” that include any nucleic acids that may be transcribed to yield target polynucleotide-specific siRNA polynucleotides (i.e., siRNA specific for a polynucleotide that encodes a target polypeptide, such as a mRNA) according to the invention as provided above; to host cells which are genetically engineered with vectors and/or constructs of the invention and to the production of siRNA polynucleotides, polypeptides, and/or fusion proteins of the invention, or fragments or variants thereof, by recombinant techniques. SiRNA sequences disclosed herein as RNA polynucleotides may be engineered to produce corresponding DNA sequences using well established methodologies such as those described herein. Thus, for example, a DNA polynucleotide may be generated from any siRNA sequence described herein (including in the Sequence Listing), such that the present siRNA sequences will be recognized as also providing corresponding DNA polynucleotides (and their complements). These DNA polynucleotides are therefore encompassed within the contemplated invention, for example, to be incorporated into the subject invention recombinant nucleic acid constructs from which siRNA may be transcribed.

[0113] According to the present invention, a vector may comprise a recombinant nucleic acid construct containing one or more promoters for transcription of an RNA molecule, for example, the human U6 snRNA promoter (see, e.g., Miyagishi et al, Nat. Biotechnol. 20:497-500 (2002); Lee et al., Nat. Biotechnol. 20:500-505 (2002); Paul et al., Nat. Biotechnol. 20:505-508 (2002); Grabarek et al., BioTechniques 34:73544 (2003); see also Sui et al., Proc. Natl. Acad. Sci. USA 99:5515-20 (2002)). Each strand of a siRNA polynucleotide may be transcribed separately each under the direction of a separate promoter and then may hybridize within the cell to form the siRNA polynucleotide duplex. Each strand may also be transcribed from separate vectors (see Lee et al., supra). Alternatively, the sense and antisense sequences specific for a PTP1B sequence may be transcribed under the control of a single promoter such that the siRNA polynucleotide forms a hairpin molecule (Paul et al., supra). In such an instance, the complementary strands of the siRNA specific sequences are separated by a spacer that comprises at least four nucleotides, but may comprise at least 5, 6, 7, 8, 9, 10, 11, 12, 14, 16, 94 18 nucleotides or more nucleotides as described herein. In addition, siRNAs transcribed under the control of a U6 promoter that form a hairpin may have a stretch of about four uridines at the 3′ end that act as the transcription termination signal (Miyagishi et al., supra; Paul et al., supra). By way of illustration, if the target sequence is 19 nucleotides, the siRNA hairpin polynucleotide (beginning at the 5′ end) has a 19-nucleotide sense sequence followed by a spacer (which as two uridine nucleotides adjacent to the 3′ end of the 19-nucleotide sense sequence), and the spacer is linked to a 19 nucleotide antisense sequence followed by a 4-uridine terminator sequence, which results in an overhang. SiRNA polynucleotides with such overhangs effectively interfere with expression of the target polypeptide (see id.). A recombinant construct may also be prepared using another RNA polymerase III promoter, the H1 RNA promoter, that may be operatively linked to siRNA polynucleotide specific sequences, which may be used for transcription of hairpin structures comprising the siRNA specific sequences or separate transcription of each strand of a siRNA duplex polynucleotide (see, e.g., Brummelkamp et al., Science 296:550-53 (2002); Paddison et al., supra). DNA vectors useful for insertion of sequences for transcription of an siRNA polynucleotide include pSUPER vector (see, e.g., Brummelkamp et al., supra); pAV vectors derived from pCWRSVN (see, e.g., Paul et al., supra); and pIND (see, e.g., Lee et al., supra), or the like.

[0114] PTP polypeptides and other target polypeptides of interest can be expressed in mammalian cells, yeast, bacteria, or other cells under the control of appropriate promoters, providing ready systems for evaluation of siRNA polynucleotides that are capable of interfering with polypeptide expression as provided herein. Appropriate cloning and expression vectors for use with prokaryotic and eukaryotic hosts are described, for example, by Sambrook, et al., Molecular Cloning: A Laboratory Manual, Third Edition, Cold Spring Harbor, N.Y., (2001).

[0115] Generally, recombinant expression vectors for use in the preparation of recombinant nucleic acid constructs or vectors of the invention will include origins of replication and selectable markers permitting transformation of the host cell, e.g., the ampicillin resistance gene of E. coli and S. cerevisiae TRP1 gene, and a promoter derived from a highly-expressed gene to direct transcription of a downstream structural sequence (e.g., a siRNA polynucleotide sequence). Such promoters can be derived from operons encoding glycolytic enzymes such as 3-phosphoglycerate kinase (PGK), α-factor, acid phosphatase, or heat shock proteins, among others. For PTP polypeptide expression (including PTP fusion proteins and substrate trapping mutant PTPs), and for other expression of other polypeptides of interest, the heterologous structural sequence is assembled in appropriate phase with translation initiation and termination sequences. Optionally, the heterologous sequence can encode a fusion protein including an N-terminal identification peptide imparting desired characteristics, e.g., stabilization or simplified purification of expressed recombinant product.

[0116] Useful expression constructs for bacterial use are constructed by inserting into an expression vector a structural DNA sequence encoding a desired siRNA polynucleotide, together with suitable transcription initiation and termination signals in operable linkage, for example, with a functional promoter. The construct may comprise one or more phenotypic selectable markers and an origin of replication to ensure maintenance of the vector construct and, if desirable, to provide amplification within the host. Suitable prokaryotic hosts for transformation include E. coli, Bacillus subtilis, Salmonella typhimurium and various species within the genera Pseudomonas, Streptomyces, and Staphylococcus, although others may also be employed as a matter of choice. Any other plasmid or vector may be used as long as they are replicable and viable in the host.

[0117] As a representative but nonlimiting example, useful expression vectors for bacterial use can comprise a selectable marker and bacterial origin of replication derived from commercially available plasmids comprising genetic elements of the well known cloning vector pBR322 (ATCC 37017). Such commercial vectors include, for example, pKK223-3 (Pharmacia Fine Chemicals, Uppsala, Sweden) and GEM1 (Promega Biotec, Madison, Wis., USA). These pBR322 “backbone” sections are combined with an appropriate promoter and the structural sequence to be expressed.

[0118] Following transformation of a suitable host strain and growth of the host strain to an appropriate cell density, the selected promoter, if it is a regulated promoter as provided herein, is induced by appropriate means (e.g., temperature shift or chemical induction) and cells are cultured for an additional period. Cells are typically harvested by centrifugation, disrupted by physical or chemical means, and the resulting crude extract retained for further purification. Microbial cells employed in expression of proteins can be disrupted by any convenient method, including freeze-thaw cycling, sonication, mechanical disruption, or use of cell lysing agents; such methods are well know to those skilled in the art.

[0119] Thus, for example, the nucleic acids of the invention as described herein (e.g., DNA sequences from which siRNA may be transcribed) herein may be included in any one of a variety of expression vector constructs as a recombinant nucleic acid construct for expressing a target polynucleotide-specific siRNA polynucleotide. Such vectors and constructs include chromosomal, nonchromosomal and synthetic DNA sequences, e.g., derivatives of SV40; bacterial plasmids; phage DNA; baculovirus; yeast plasmids; vectors derived from combinations of plasmids and phage DNA, viral DNA, such as vaccinia, adenovirus, fowl pox virus, and pseudorabies. However, any other vector may be used for preparation of a recombinant nucleic acid construct as long as it is replicable and viable in the host.

[0120] The appropriate DNA sequence(s) may be inserted into the vector by a variety of procedures. In general, the DNA sequence is inserted into an appropriate restriction endonuclease site(s) by procedures known in the art. Standard techniques for cloning, DNA isolation, amplification and purification, for enzymatic reactions involving DNA ligase, DNA polymerase, restriction endonucleases and the like, and various separation techniques are those known and commonly employed by those skilled in the art. A number of standard techniques are described, for example, in Ausubel et al. (1993 Current Protocols in Molecular Biology, Greene Publ. Assoc. Inc. & John Wiley & Sons, Inc., Boston, Mass.); Sambrook et al. (2001 Molecular Cloning, Third Ed., Cold Spring Harbor Laboratory, Plainview, N.Y.); Maniatis et al. (1982 Molecular Cloning, Cold Spring Harbor Laboratory, Plainview, N.Y.); and elsewhere.

[0121] The DNA sequence in the expression vector is operatively linked to at least one appropriate expression control sequences (e.g., a promoter or a regulated promoter) to direct mRNA synthesis. Representative examples of such expression control sequences include LTR or SV40 promoter, the E. coli lac or trp, the phage lambda PL promoter and other promoters known to control expression of genes in prokaryotic or eukaryotic cells or their viruses. Promoter regions can be selected from any desired gene using CAT (chloramphenicol transferase) vectors or other vectors with selectable markers. Two appropriate vectors are pKK232-8 and pCM7. Particular named bacterial promoters include lac, lacZ, T3, T7, gpt, lambda P_(R), P_(L) and trp. Eukaryotic promoters include CMV immediate early, HSV thymidine kinase, early and late SV40, LTRs from retrovirus, and mouse metallothionein-I. Selection of the appropriate vector and promoter is well within the level of ordinary skill in the art, and preparation of certain particularly preferred recombinant expression constructs comprising at least one promoter or regulated promoter operably linked to a nucleic acid encoding a polypeptide (e.g., PTP, MAP kinase kinase, or chemotherapeutic target polypeptide) is described herein.

[0122] As noted above, in certain embodiments the vector may be a viral vector such as a retroviral vector. For example, retroviruses from which the retroviral plasmid vectors may be derived include, but are not limited to, Moloney Murine Leukemia Virus, spleen necrosis virus, retroviruses such as Rous Sarcoma Virus, Harvey Sarcoma virus, avian leukosis virus, gibbon ape leukemia virus, human immunodeficiency virus, adenovirus, Myeloproliferative Sarcoma Virus, and mammary tumor virus.

[0123] The viral vector includes one or more promoters. Suitable promoters which may be employed include, but are not limited to, the retroviral LTR; the SV40 promoter; and the human cytomegalovirus (CMV) promoter described in Miller, et al., Biotechniques 7:980-990 (1989), or any other promoter (e.g., cellular promoters such as eukaryotic cellular promoters including, but not limited to, the histone, pol III, and β-actin promoters). Other viral promoters which may be employed include, but are not limited to, adenovirus promoters, thymidine kinase (TK) promoters, and B19 parvovirus promoters. The selection of a suitable promoter will be apparent to those skilled in the art from the teachings contained herein, and may be from among either regulated promoters or promoters as described above.

[0124] The retroviral plasmid vector is employed to transduce packaging cell lines to form producer cell lines. Examples of packaging cells which may be transfected include, but are not limited to, the PE501, PA317, ψ-2, ψ-AM, PA12, T19-14X, VT-19-17-H2, ψCRE, ψCRIP, GP+E-86, GP+envAm12, and DAN cell lines as described in Miller, Human Gene Therapy, 1:5-14 (1990), which is incorporated herein by reference in its entirety. The vector may transduce the packaging cells through any means known in the art. Such means include, but are not limited to, electroporation, the use of liposomes, and calcium phosphate precipitation. In one alternative, the retroviral plasmid vector may be encapsulated into a liposome, or coupled to a lipid, and then administered to a host.

[0125] The producer cell line generates infectious retroviral vector particles that include the nucleic acid sequence(s) encoding the PTP polypeptides or other polypeptide of interest and fusion proteins thereof. Such retroviral vector particles then may be employed, to transduce eukaryotic cells, either in vitro or in vivo. The transduced eukaryotic cells will express the nucleic acid sequence(s) encoding the siRNA polynucleotide that is capable of specifically interfering with expression of a polypeptide or fusion protein. Eukaryotic cells which may be transduced include, but are not limited to, embryonic stem cells, embryonic carcinoma cells, as well as hematopoietic stem cells, hepatocytes, fibroblasts, myoblasts, keratinocytes, endothelial cells, bronchial epithelial cells and various other culture-adapted cell lines.

[0126] In another aspect, the present invention relates to host cells containing the above described recombinant PTP expression constructs and to host cells containing the above described recombinant expression constructs comprising a (non-PTP) polypeptide of interest as described herein. Host cells are genetically engineered (transduced, transformed or transfected) with the vectors and/or expression constructs of this invention that may be, for example, a cloning vector, a shuttle vector, or an expression construct. The vector or construct may be, for example, in the form of a plasmid, a viral particle, a phage, etc. The engineered host cells can be cultured in conventional nutrient media modified as appropriate for activating promoters, selecting transformants or amplifying particular genes such as genes encoding siRNA polynucleotides or fusion proteins thereof. The culture conditions for particular host cells selected for expression, such as temperature, pH and the like, will be readily apparent to the ordinarily skilled artisan.

[0127] The host cell can be a higher eukaryotic cell, such as a mammalian cell, or a lower eukaryotic cell, such as a yeast cell, or the host cell can be a prokaryotic cell, such as a bacterial cell. Representative examples of appropriate host cells according to the present invention include, but need not be limited to, bacterial cells, such as E. coli, Streptomyces, Salmonella typhimurium; fungal cells, such as yeast; insect cells, such as Drosophila S2 and Spodoptera S19; animal cells, such as CHO, COS or 293 cells; adenoviruses; plant cells, or any suitable cell already adapted to in vitro propagation or so established de novo. The selection of an appropriate host is deemed to be within the scope of those skilled in the art from the teachings herein.

[0128] Various mammalian cell culture systems can also be employed to produce siRNA polynucleotides from recombinant nucleic acid constructs of the present invention. The invention is therefore directed in part to a method of producing a siRNA polynucleotide, by culturing a host cell comprising a recombinant nucleic acid construct that comprises at least one promoter operably linked to a nucleic acid sequence encoding a siRNA polynucleotide specific for a desired target polypeptide. In certain embodiments, the promoter may be a regulated promoter as provided herein, for example a tetracylcine-repressible promoter. In certain embodiments the recombinant expression construct is a recombinant viral expression construct as provided herein. Examples of mammalian expression systems include the COS-7 lines of monkey kidney fibroblasts, described by Gluzman, Cell 23:175 (1981), and other cell lines capable of expressing a compatible vector, for example, the C127, 3T3, CHO, HeLa, HEK, and BHK cell lines. Mammalian expression vectors will comprise an origin of replication, a suitable promoter and enhancer, and also any necessary ribosome binding sites, polyadenylation site, splice donor and acceptor sites, transcriptional termination sequences, and 5′ flanking nontranscribed sequences, for example as described herein regarding the preparation of recombinant siRNA polynucleotide constructs. DNA sequences derived from the SV40 splice, and polyadenylation sites may be used to provide the required nontranscribed genetic elements. Introduction of the construct into the host cell can be effected by a variety of methods with which those skilled in the art will be familiar, including but not limited to, for example, liposomes including cationic liposomes, calcium phosphate transfection, DEAF-Dextran mediated transfection, or electroporation (Davis et al., 1986 Basic Methods in Molecular Biology), or other suitable technique.

[0129] The expressed recombinant siRNA polynucleotides may be useful in intact host cells; in intact organelles such as cell membranes, intracellular vesicles or other cellular organelles; or in disrupted cell preparations including but not limited to cell homogenates or lysates, microsomes, uni- and multilamellar membrane vesicles or other preparations. Alternatively, expressed recombinant siRNA polynucleotides can be recovered and purified from recombinant cell cultures by methods including ammonium sulfate or ethanol precipitation, acid extraction, anion or cation exchange chromatography, phosphocellulose chromatography, hydrophobic interaction chromatography, affinity chromatography, hydroxylapatite chromatography and lectin chromatography. Finally, high performance liquid chromatography (HPLC) can be employed for final purification steps.

[0130] Samples

[0131] According to the present invention, a method is provided for interfering with expression of a desired target polypeptide as provided herein, comprising contacting a siRNA polynucleotide with a cell that is capable of expressing the target polypeptide, typically in a biological sample or in a subject or biological source. A “sample” as used herein refers to a biological sample containing at least one protein tyrosine phosphatase or a MAP kinase kinase or a chemotherapeutic target polypeptide, and may be provided by obtaining a blood sample, biopsy specimen, tissue explant, organ culture or any other tissue or cell preparation from a subject or a biological source. A sample may further refer to a tissue or cell preparation in which the morphological integrity or physical state has been disrupted, for example, by dissection, dissociation, solubilization, fractionation, homogenization, biochemical or chemical extraction, pulverization, lyophilization, sonication or any other means for processing a sample derived from a subject or biological source. In certain preferred embodiments, the sample is a cell that comprises at least one PTP and/or at least one MAP kinase, and/or at least one MAP kinase kinase, and in certain particularly preferred embodiments the cell comprises an inducible biological signaling pathway, at least one component of which is a specific target polypeptidee. In particularly preferred embodiments the cell is a mammalian cell, for example, Rat-1 fibroblasts, COS cells, CHO cells, HEK-293 cells, HepG2, HII4E-C3, L6, and 3T3-L1, or other well known model cell lines, which are available from the American Type Culture Collection (ATCC, Manassas, Va.). In other preferred embodiments, the cell line is derived from PTP-1B knockout animals and which may be transfected with human insulin receptor (HIR), for example, 1BKO mouse embryo fibroblasts.

[0132] In certain other preferred embodiments the sample is a cell that comprises a chemotherapeutic target polypeptide, which includes, for example, a cell line that is derived from a tumor cell. The cell line may be a primary tumor cell line, that is, a cell line prepared directly from a tumor sample removed from a human or a non-human animal. Alternatively, the cell line may be one of several established tumor cell lines known in the art, including but not limited to MCF7, T47D, SW620, HS578T, MDA-MB-435, MDA MB 231, HCT-116, HT-29, HeLa, Raji, Ramos, and the like (see ATCC collection).

[0133] The subject or biological source may be a human or non-human animal, a primary cell culture or culture adapted cell line including but not limited to genetically engineered cell lines that may contain chromosomally integrated or episomal recombinant nucleic acid sequences, immortalized or immortalizable cell lines, somatic cell hybrid cell lines, differentiated or differentiatable cell lines, transformed cell lines and the like. Optionally, in certain situations it may be desirable to treat cells in a biological sample with hydrogen peroxide and/or with another agent that directly or indirectly promotes reactive oxygen species (ROS) generation, including biological stimuli as described herein; in certain other situations it may be desirable to treat cells in a biological sample with a ROS scavenger, such as N-acetyl cysteine (NAC) or superoxide dismutase (SOD) or other ROS scavengers known in the art; in other situations cellular glutathione (GSH) may be depleted by treating cells with L-buthionine-SR-sulfoximine (Bso); and in other circumstances cells may be treated with pervanadate to enrich the sample in tyrosine phosphorylated proteins. Other means may also be employed to effect an increase in the population of tyrosine phosphorylated proteins present in the sample, including the use of a subject or biological source that is a cell line that has been transfected with at least one gene encoding a protein tyrosine kinase.

[0134] Additionally or alternatively, a biological signaling pathway may be induced in subject or biological source cells by contacting such cells with an appropriate stimulus, which may vary depending upon the signaling pathway under investigation, whether known or unknown. For example, a signaling pathway that, when induced, results in protein tyrosine phosphorylation and/or protein tyrosine dephosphorylation may be stimulated in subject or biological source cells using any one or more of a variety of well known methods and compositions known in the art to stimulate protein tyrosine kinase (PTK) and/or PTP activity. These stimuli may include, without limitation, exposure of cells to cytokines, growth factors, hormones, peptides, small molecule mediators, cell stressors (e.g., ultraviolet light; temperature shifts; osmotic shock; ROS or a source thereof, such as hydrogen peroxide, superoxide, ozone, etc. or any agent that induces or promotes ROS production (see, e.g., Halliwell and Gutteridge, Free Radicals in Biology and Medicine (3^(rd) Ed.) 1999 Oxford University Press, Oxford, UK); heavy metals; alcohol) or other agents that induce PTK-mediated protein tyrosine phosphorylation and/or PTP-mediated phosphoprotein tyrosine dephosphorylation. Such agents may include, for example, interleukins (e.g., IL-1, IL-3), interferons (e.g., IFN-γ), human growth hormone, insulin, epidermal growth factor (EGF), platelet derived growth factor (PDGF), granulocyte colony stimulating factor (G-CSF), granulocyte-megakaryocyte colony stimulating factor (GM-CSF), transforming growth factor (e.g., TGF-β1), tumor necrosis factor (e.g., TNF-α) and fibroblast growth factor (FGF; e.g., basic FGF (bFGF)), any agent or combination of agents capable of triggering T lymphocyte activation via the T cell receptor for antigen (TCR; TCR-inducing agents may include superantigens, specifically recognized antigens and/or MHC-derived peptides, MHC peptide tetramers (e.g., Altman et al., 1996 Science 274:94-96); TCR-specific antibodies or fragments or derivatives thereof), lectins (e.g., PHA, PWM, ConA, etc.), mitogens, G-protein coupled receptor agonists such as angiotensin-2, thrombin, thyrotropin, parathyroid hormone, lysophosphatidic acid (LPA), sphingosine-1-phosphate, serotonin, endothelin, acetylcholine, platelet activating factor (PAF) or bradykinin, as well as other agents with which those having ordinary skill in the art will be familiar (see, e.g., Rhee et al., [online] Oct. 10, 2000 Science's stke, Internet:URL<www.stke.org/cgl/content/full/OC_sigtrans;2000/53/pel>), and references cited therein).

[0135] As noted above, regulated tyrosine phosphorylation contributes to specific pathways for biological signal transduction, including those associated with cell division, cell survival, apoptosis, proliferation and differentiation, and “inducible signaling pathways” in the context of the present invention include transient or stable associations or interactions among molecular components involved in the control of these and similar processes in cells. Depending on the particular pathway of interest, an appropriate parameter for determining induction of such pathway may be selected. For example, for signaling pathways associated with cell proliferation, a variety of well known methodologies are available for quantifying proliferation, including, for example, incorporation of tritiated thymidine into cellular DNA, monitoring of detectable (e.g., fluorimetric or colorimetric) indicators of cellular respiratory activity, (e.g., MTT assay) or cell counting, or the like. Similarly, in the cell biology arts there are known multiple techniques for assessing cell survival (e.g., vital dyes, metabolic indicators, etc.) and for determining apoptosis (e.g., annexin V binding, DNA fragmentation assays, caspase activation, PARP cleavage, etc.). Other signaling pathways will be associated with particular cellular phenotypes, for example specific induction of gene expression (e.g., detectable as transcription or translation products, or by bioassays of such products, or as nuclear localization of cytoplasmic factors), altered (e.g., statistically significant increases or decreases) levels of intracellular mediators (e.g., activated kinases or phosphatases, altered levels of cyclic nucleotides or of physiologically active ionic species, etc.), altered cell cycle profiles, or altered cellular morphology, and the like, such that cellular responsiveness to a particular stimulus as provided herein can be readily identified to determine whether a particular cell comprises an inducible signaling pathway.

[0136] In preferred embodiments where a siRNA of the invention is being used to interfere with expression of a target polypeptide that is a PTP or that is a component of a biological signaling pathway that comprises a PTP, a PTP substrate may be any naturally or non-naturally occurring phosphorylated peptide, polypeptide or protein that can specifically bind to and/or be dephosphorylated by a PTP (including dual specificity phosphatases) as provided herein, or any other phosphorylated molecule that can be a substrate of a PTP family member as provided herein. Non-limiting examples of known PTP substrates include the proteins VCP (see, e.g., Zhang et al., 1999 J. Biol. Chem. 274:17806, and references cited therein), p130^(cas), EGF receptor, p210 bcr:abl, MAP kinase, Shc (Tiganis et al., 1998 Mol Cell. Biol. 18:1622-1634), insulin receptor, lck (lymphocyte specific protein tyrosine kinase, Marth et al., 1985 Cell 43:393), T cell receptor zeta chain, and phosphatidylinositol 3,4,5-triphosphate (Maehama et al., 1998 J. Biol. Chem. 273:13375).

[0137] Identification and selection of PTP substrates as provided herein, for use in the present invention, may be performed according to procedures with which those having ordinary skill in the art will be familiar, or may, for example, be conducted according to the disclosures of WO 00/75339, U.S. application Ser. No. 09/334,575, or U.S. application Ser. No. 10/366,547, and references cited therein. The phosphorylated protein/PTP complex may be isolated, for example, by conventional isolation techniques as described in U.S. Pat. No. 5,352,660, including salting out, chromatography, electrophoresis, gel filtration, fractionation, absorption, polyacrylamide gel electrophoresis, agglutination, combinations thereof or other strategies. PTP substrates that are known may also be prepared according to well known procedures that employ principles of molecular biology and/or peptide synthesis (e.g., Ausubel et al., Current Protocols in Molecular Biology, Greene Publ. Assoc. Inc. & John Wiley & Sons, Inc., Boston, Mass. (1993); Sambrook et al., Molecular Cloning, Third Ed., Cold Spring Harbor Laboratory, Plainview, N.Y. (2001); Fox, Molec. Biotechnol. 3:249 (1995); Maeji et al., Pept. Res. 8:33 (1995)).

[0138] The PTP substrate peptides of the present invention may therefore be derived from PTP substrate proteins, polypeptides and peptides as provided herein having amino acid sequences that are identical or similar to tyrosine phosphorylated PTP substrate sequences known in the art. For example by way of illustration and not limitation, peptide sequences derived from the known PTP substrate proteins referred to above are contemplated for use according to the instant invention, as are peptides having at least 70% similarity (preferably 70% identity), more preferably 80% similarity (more preferably 80% identity), more preferably 90% similarity (more preferably 90% identity) and still more preferably 95% similarity (still more preferably 95% identity) to the polypeptides described in references cited herein and in the Examples and to portions of such polypeptides as disclosed herein. As known in the art “similarity” between two polypeptides is determined by comparing the amino acid sequence and conserved amino acid substitutes thereto of the polypeptide to the sequence of a second polypeptide (e.g., using GENEWORKS, Align or the BLAST algorithm, or another algorithm, as described above).

[0139] In certain preferred embodiments of the present invention, the siRNA polynucleotide and/or the PTP substrate is detectably labeled, and in particularly preferred embodiments the siRNA polynucleotide and/or PTP substrate is capable of generating a radioactive or a fluorescent signal. The siRNA polynucleotide and/or PTP substrate can be detectably labeled by covalently or non-covalently attaching a suitable reporter molecule or moiety, for example a radionuclide such as ³²P (e.g., Pestka et al., 1999 Protein Expr. Purif. 17:203-14), a radiohalogen such as iodine [¹²⁵I or ¹³¹I] (e.g., Wilbur, 1992 Bioconjug. Chem. 3:433-70), or tritium [³H]; an enzyme; or any of various luminescent (e.g., chemiluminescent) or fluorescent materials (e.g., a fluorophore) selected according to the particular fluorescence detection technique to be employed, as known in the art and based upon the present disclosure. Fluorescent reporter moieties and methods for labeling siRNA polynucleotides and/or PTP substrates as provided herein can be found, for example in Haugland (1996 Handbook of Fluorescent Probes and Research Chemicals—Sixth Ed., Molecular Probes, Eugene, Oreg.; 1999 Handbook of Fluorescent Probes and Research Chemicals—Seventh Ed., Molecular Probes, Eugene, Oreg., Internet: http://www.probes.com/lit/) and in references cited therein. Particularly preferred for use as such a fluorophore in the subject invention methods are fluorescein, rhodamine, Texas Red, AlexaFluor-594, AlexaFluor-488, Oregon Green, BODIPY-FL, umbelliferone, dichlorotriazinylamine fluorescein, dansyl chloride, phycoerythrin or Cy-5. Examples of suitable enzymes include, but are not limited to, horseradish peroxidase, biotin, alkaline phosphatase, β-galactosidase and acetylcholinesterase. Appropriate luminescent materials include luminol, and suitable radioactive materials include radioactive phosphorus [³²P]. In certain other preferred embodiments of the present invention, a detectably labeled siRNA polynucleotide comprises a magnetic particle, for example a paramagnetic or a diamagnetic particle or other magnetic particle or the like (preferably a microparticle) known to the art and suitable for the intended use. Without wishing to be limited by theory, according to certain such embodiments there is provided a method for selecting a cell that has bound, adsorbed, absorbed, internalized or otherwise become associated with a siRNA polynucleotide that comprises a magnetic particle. For example, selective isolation of a population or subpopulation of cells containing one or more PTP-specific siRNA polynucleotide-magnetic particle conjugates may offer certain advantages in the further characterization or regulation of PTP signaling pathways.

[0140] In certain embodiments of the present invention, particular PTP-specific siRNA polynucleotides of interest may be identified by contacting a candidate siRNA polynucleotide with a sample comprising a cell that comprises a target polypeptide-encoding gene and that is capable of target polypeptide gene transcription or expression (e.g., translation), under conditions and for a time sufficient to detect such gene transcription or expression, and comparing target transcription levels, polypeptide expression and/or functional expression (e.g., PTP catalytic activity) in the absence and presence of the candidate siRNA polynucleotide. Preferably target transcription or expression is decreased in the presence of the siRNA polynucleotide, which in the case of targets that are PTPs provides an alternative to PTP active site directed approaches to modulating PTP activity. (The invention need not be so limited, however, and contemplates other embodiments wherein transcription and/or expression levels of a signal transduction component other than that which is specifically targeted by the siRNA may be increased in the presence of a certain target-specific siRNA polynucleotide. By way of non-limiting theory, such an increase may result from a cellular compensatory mechanism that is induced as a result of the siRNA.)

[0141] Activity of a siRNA target polypeptide of interest may also be measured in whole cells transfected with a reporter gene whose expression is dependent upon the activation of an appropriate substrate. For example, appropriate cells (i.e., cells that express the target polypeptide and that have also been transfected with a target-specific siRNA polynucleotide that is either known or suspected of being capable of interfering with target polypeptide expression) may be transfected with a substrate-dependent promoter linked to a reporter gene. In such a system, expression of the reporter gene (which may be readily detected using methods well known to those of ordinary skill in the art) depends upon activation of the substrate via its interaction with the target polypeptide. For example, dephosphorylation of substrate may be detected based on a decrease in reporter activity in situations where the target polypeptide regulates substrate phosphorylation.

[0142] Within other aspects, the present invention provides animal models in which an animal, by virtue of introduction of an appropriate target polypeptide-specific siRNA polynucleotide, for example, as a transgene, does not express (or expresses a significantly reduced amount of) a functional PTP. Such animals may be generated, for example, using standard homologous recombination strategies, or alternatively, for instance, by oocyte microinjection with a plasmid comprising the siRNA-encoding sequence that is regulated by a suitable promoter (e.g., ubiquitous or tissue-specific) followed by implantation in a surrogate mother. Animal models generated in this manner may be used to study activities of PTP signaling pathway components and modulating agents in vivo.

[0143] Therapeutic Methods

[0144] One or more siRNA polynucleotides capable of interfering with target polypeptide expression and identified according to the above-described methods may also be used to modulate (e.g., inhibit or potentiate) target polypeptide activity in a patient. As used herein, a “patient” may be any mammal, including a human, and may be afflicted with a condition associated with undesired target polypeptide activity or may be free of detectable disease. Accordingly, the treatment may be of an existing disease or may be prophylactic. Conditions associated with signal transduction and/or with inappropriate activity of specific siRNA target polypeptides described herein include obesity, impaired glucose tolerance and diabetes and cancer, disorders associated with cell proliferation, including cancer, graft-versus-host disease (GVHD), autoimmune diseases, allergy or other conditions in which immunosuppression may be involved, metabolic diseases, abnormal cell growth or proliferation and cell cycle abnormalities.

[0145] For administration to a patient, one or more specific siRNA polynucleotides, either alone, with or without chemical modification or removal of ribose, or comprised in an appropriate vector as described herein (e.g., including a vector which comprises a DNA sequence from which a specific siRNA can be transcribed) are generally formulated as a pharmaceutical composition. A pharmaceutical composition may be a sterile aqueous or non-aqueous solution, suspension or emulsion, which additionally comprises a physiologically acceptable carrier (i.e., a non-toxic material that does not interfere with the activity of the active ingredient). Such compositions may be in the form of a solid, liquid or gas (aerosol). Alternatively, compositions of the present invention may be formulated as a lyophilizate or compounds may be encapsulated within liposomes using well known technology. Pharmaceutical compositions within the scope of the present invention may also contain other components, which may be biologically active or inactive. Such components include, but are not limited to, buffers (e.g., neutral buffered saline or phosphate buffered saline), carbohydrates (e.g., glucose, mannose, sucrose or dextrans), mannitol, proteins, polypeptides or amino acids such as glycine, antioxidants, chelating agents such as EDTA or glutathione, stabilizers, dyes, flavoring agents, and suspending agents and/or preservatives.

[0146] Any suitable carrier known to those of ordinary skill in the art may be employed in the pharmaceutical compositions of the present invention. Carriers for therapeutic use are well known, and are described, for example, in Remingtons Pharmaceutical Sciences, Mack Publishing Co. (A. R. Gennaro ed. 1985). In general, the type of carrier is selected based on the mode of administration. Pharmaceutical compositions may be formulated for any appropriate manner of administration, including, for example, topical, oral, nasal, intrathecal, rectal, vaginal, sublingual or parenteral administration, including subcutaneous, intravenous, intramuscular, intrasternal, intracavernous, intrameatal or intraurethral injection or infusion. For parenteral administration, the carrier preferably comprises water, saline, alcohol, a fat, a wax or a buffer. For oral administration, any of the above carriers or a solid carrier, such as mannitol, lactose, starch, magnesium stearate, sodium saccharine, talcum, cellulose, kaolin, glycerin, starch dextrins, sodium alginate, carboxymethylcellulose, ethyl cellulose, glucose, sucrose and/or magnesium carbonate, may be employed.

[0147] A pharmaceutical composition (e.g., for oral administration or delivery by injection) may be in the form of a liquid (e.g., an elixir, syrup, solution, emulsion or suspension). A liquid pharmaceutical composition may include, for example, one or more of the following: sterile diluents such as water for injection, saline solution, preferably physiological saline, Ringer's solution, isotonic sodium chloride, fixed oils such as synthetic mono or diglycerides which may serve as the solvent or suspending medium, polyethylene glycols, glycerin, propylene glycol or other solvents; antibacterial agents such as benzyl alcohol or methyl paraben; antioxidants such as ascorbic acid or sodium bisulfite; chelating agents such as ethylenediaminetetraacetic acid; buffers such as acetates, citrates or phosphates and agents for the adjustment of tonicity such as sodium chloride or dextrose. A parenteral preparation can be enclosed in ampoules, disposable syringes or multiple dose vials made of glass or plastic. The use of physiological saline is preferred, and an injectable pharmaceutical composition is preferably sterile.

[0148] The compositions described herein may be formulated for sustained release (i.e., a formulation such as a capsule or sponge that effects a slow release of compound following administration). Such compositions may generally be prepared using well known technology and administered by, for example, oral, rectal or subcutaneous implantation, or by implantation at the desired target site. Sustained-release formulations may contain an agent dispersed in a carrier matrix and/or contained within a reservoir surrounded by a rate controlling membrane. Carriers for use within such formulations are biocompatible, and may also be biodegradable; preferably the formulation provides a relatively constant level of active component release. The amount of active compound contained within a sustained release formulation depends upon the site of implantation, the rate and expected duration of release and the nature of the condition to be treated or prevented.

[0149] Within a pharmaceutical composition, a therapeutic agent comprising a polypeptide-directed siRNA polynucleotide as described herein (or, e.g., a recombinant nucleic acid construct encoding a siRNA polynucleotide) may be linked to any of a variety of compounds. For example, such an agent may be linked to a targeting moiety (e.g., a monoclonal or polyclonal antibody, a protein or a liposome) that facilitates the delivery of the agent to the target site. As used herein, a “targeting moiety” may be any substance (such as a compound or cell) that, when linked to an agent enhances the transport of the agent to a target cell or tissue, thereby increasing the local concentration of the agent. Targeting moieties include antibodies or fragments thereof, receptors, ligands and other molecules that bind to cells of, or in the vicinity of, the target tissue. An antibody targeting agent may be an intact (whole) molecule, a fragment thereof, or a functional equivalent thereof. Examples of antibody fragments are F(ab′)₂, Fab′, Fab and F[v] fragments, which may be produced by conventional methods or by genetic or protein engineering. Linkage is generally covalent and may be achieved by, for example, direct condensation or other reactions, or by way of bi- or multi-functional linkers. Targeting moieties may be selected based on the cell(s) or tissue(s) toward which the agent is expected to exert a therapeutic benefit.

[0150] Pharmaceutical compositions may be administered in a manner appropriate to the disease to be treated (or prevented). An appropriate dosage and a suitable duration and frequency of administration will be determined by such factors as the condition of the patient, the type and severity of the patient's disease, the particular form of the active ingredient and the method of administration. In general, an appropriate dosage and treatment regimen provides the agent(s) in an amount sufficient to provide therapeutic and/or prophylactic benefit (e.g., an improved clinical outcome, such as more frequent complete or partial remissions, or longer disease-free and/or overall survival, or a lessening of symptom severity). For prophylactic use, a dose should be sufficient to prevent, delay the onset of or diminish the severity of a disease associated with cell proliferation.

[0151] Optimal dosages may generally be determined using experimental models and/or clinical trials. In general, the amount of siRNA polynucleotide present in a dose, or produced in situ by DNA present in a dose (e.g., from a recombinant nucleic acid construct comprising a siRNA polynucleotide), ranges from about 0.01 μg to about 1001 g per kg of host, typically from about 0.1 μg to about 10 μg. The use of the minimum dosage that is sufficient to provide effective therapy is usually preferred. Patients may generally be monitored for therapeutic or prophylactic effectiveness using assays suitable for the condition being treated or prevented, which will be familiar to those having ordinary skill in the art. Suitable dose sizes will vary with the size of the patient, but will typically range from about 10 mL to about 500 mL for 10-60 kg animal.

[0152] The following Examples are offered by way of illustration and not by way of limitation.

EXAMPLE 1 Interference of Dual Specificity Phosphatase Expression by Small Interfering RNA

[0153] This example describes the effect on dual specificity phosphatase (DSP) expression in cells transfected with sequence-specific small interfering RNA (siRNA) polynucleotides. Interference with expression of MKP-1 and DSP-3 was examined by transfecting sequence-specific siRNAs into mammalian cells expressing the DSP polypeptide and then detecting expression by immunoblot.

[0154] The siRNA nucleotide sequences specific for each DSP were chosen by first scanning the open reading frame of the target cDNA for 21-base sequences that were flanked on the 5′ end by two adenine bases (AA) and that had A+T/G+C ratios that were nearly 1:1. Twenty-one-base sequences with an A+T/G+C ratio greater than 2:1 or 1:2 were excluded. If no 21-base sequences were identified that met this criteria, the polynucleotide sequence encoding the DSP was searched for a 21-base sequence having the bases CA at the 5′ end. The polynucleotide sequences examined were the sequences encoding DSP-3 polypeptide (SEQ ID NO:______) and MKP-1 (SEQ ID NO:______). For the selection of sequences for some of the siRNA polynucleotides, the sense and antisense sequences of each 21-mer that met the above criteria were then analyzed to determine if the sequence had the potential to form an internal hairpin loop or homodimer. Such an analysis can be performed using computer software programs known to those in the art. Any 21-mer that had an internal hairpin loop melting temperature of greater than 55° C. and a homodimer melting temperature of greater than 37° C. was excluded. The specificity of each 21-mer was determined by performing a BLAST search of public databases. Sequences that contained at least 16 of 21 consecutive nucleotides with 100% identity with a polynucleotide sequence other than the target sequence were not used in the experiments. In each of the Examples provided herein, each siRNA sequence represents the sense strand of the siRNA polynucleotide and its corresponding sequence identifier. “Related sequence identifiers” referred to in the Examples identify sequences in the sequence listing that contain the same nucleotides at positions 1-19 of the siRNA sequence with and without two additional nucleotides (NN) at the 3′ end (which would correspond to a two-nucleotide overhang in a double stranded polynucleotide), and the reverse complement of each. Unless otherwise stated, it is to be understood that the siRNA transfected into a cell is composed of the sense strand and its complementary antisense strand, which form a duplex siRNA polynucleotide. The sequences chosen for these experiments were as follows.

[0155] DSP-3 Specific: DSP3.1: 5′-cgauagugccaggccuaugtt-3′ [SEQ ID NO:   ] DSP3.2: 5′-gcaugagguccaucaguautt-3′ [SEQ ID NO:   ] DSP3.3: 5′-cgauacugccaggcccaugtt-3′ [SEQ ID NO:   ]

[0156] MKP-1 Specific: MKP.1: 5′-auccugcccuuucuguacctt-3′ [SEQ ID NO:   ] MKP.2: 5′-gcagaggcaaagcaucauctt-3′ [SEQ ID NO:   ]

[0157] Sense and antisense oligonucleotides for MKP.1, MKP.2, DSP3.1, DSP3.2, and DSP3.3 were synthesized according to the standard protocol of the vendor (Dharmacon Research, Inc., Lafayette, Colo.). For some experiments described in this and other examples, the vendor gel-purified the double-stranded siRNA polynucleotide, which was then used. In the instances when the vendor did not prepare double-stranded siRNA, just before transfection, double-stranded siRNAs were prepared by annealing the sense and anti-sense oligonucleotides in annealing buffer (100 mM potassium acetate, 30 mM HEPES-KOH, pH 7.4, 2 mM magnesium acetate) for 1 minute at 90° C., followed by a 60 minute incubation at 37° C.

[0158] Recombinant nucleic acid expression vectors containing encoding sequences for the MKP-1 polypeptide and DSP-3 polypeptide were prepared according to standard molecular biology techniques. Polynucleotides comprising the MKP-1 coding sequence of SEQ ID NO:______ and comprising the DSP-3 coding sequence of SEQ ID NO:______ were cloned into recombinant expression vectors according to methods known to those skilled in the molecular biology art.

[0159] HeLa cells (ATCC, Manassas, Va.) were maintained in Dulbecco's modified Eagle's medium (DMEM, Life Technologies, Inc., Gaithersburg, Md.) plus 10% fetal bovine serum (FBS), 100 units/ml penicillin, and 100 μg/ml streptomycin. Cells were plated in 6-well tissue culture plates at a density of approximately 5×10⁴ cells per well at the time of transfection.

[0160] HeLa cells were transfected with 60 pmoles of MKP.1, MKP.2, or CD45.1 (SEQ ID NO:______) siRNA. For each cell culture well, the siRNA polynucleotides were diluted into 250 μl of O_(PTI)MEM® Reduced Serum Medium (Gibco™, Life Technologies), and 15 μl Oligofectamine™ (Invitrogen Life Technologies, Carlsbad, Calif.) was diluted into 250 μl of O_(PTI)MEM®. A control solution without siRNA was also prepared. Each solution was incubated at room temperature for 5 minutes. The two solutions were mixed and then incubated for 20 minutes at room temperature to allow the liposome-nucleic acid complexes to form. FBS-containing media was removed from the HeLa cell cultures and replaced with O_(PTI)MEM®. The liposome-nucleic acid mixture then was added to the HeLa cell culture, and the transfected cells incubated at 37° C. for 22-24 hours. Media were removed from the cell cultures and replaced with DMEM containing 10% FBS. Cells were incubated at 37° C. in the media plus FBS solution for 0, 1, or 4 hours.

[0161] Expression of MKP-1 was analyzed by immunoblotting HeLa cell extracts. The cells were rinsed twice in phosphate buffered saline (PBS) (4° C.) and then lysed in 250 μl of ice-cold RIPA buffer RIPA buffer (150 mM NaCl, 10 mM NaPO₄, 2 mM EDTA, 1% deoxycholate, 1% Nonidet® P40, 0.1% SDS, 5 mM NaF, 14.3 mM beta-mercaptoethanol, and Complete Protease Inhibitor (Roche Applied Bioscience, Indianapolis, Ind.). The lysates were centrifuged and aliquots of supernatant (10 μl) from each transfected cell culture sample were combined with 10 μl of 2×SDS-PAGE reducing sample buffer. The samples were heated at 95° C. for five minutes, and then applied to a 14% Tris-glycine SDS-PAGE gel (NOVEX® from Invitrogen Life Technologies, Carlsbad, Calif.). After electrophoresis, the separated proteins were electrophoretically transferred from the gel onto an Immobilon-P polyvinylidene fluoride (PVDF) membrane (Millipore, Bedford, Mass.). The PVDF membrane was blocked in 5% milk in TBST (20 mM Tris pH 7.5, 150 mM NaCl, 0.05% Tween-20), incubated with an anti-MKP-1 antibody (Santa Cruz Biotechnology, Inc., Santa Cruz, Calif.) for 2-16 hours at room temperature, washed 3×10 minutes with TBST, and then incubated with an appropriate horseradish peroxidase (HRP) conjugate IgG (1:10,000) (Amersham Biosciences, Piscataway, N.J.) for 30 minutes at room temperature. Binding was detected with the ECL chemiluminescent reagent used according to the manufacturer's instructions (Amersham Biosciences, Piscataway, N.J.) as shown in FIG. 1 (upper). A second SDS-PAGE gel in which the HeLa cell extracts were separated was stained with Coomassie Blue (FIG. 1, lower).

[0162] Interference with DSP-3 polypeptide expression was analyzed in HeLa cells transfected with siRNA polynucleotides. To determine the transfection efficiency of a siRNA polynucleotide, HeLa cells cultured as described above were plated at different cell densities and then transfected with a sequence-specific siRNA. DSP3.1 siRNA (SEQ ID NO:______) was synthesized and conjugated to fluorescein isothiocyanate (FITC) according to the vendor's standard methods (Synthetic Genetics, San Diego, Calif.). HeLa cells plated at varying cell densities to achieve approximately 1×10⁴ cells/well, 3×10⁴ cells/well, 5×10⁴ cells/well, 1×10⁵ cells/well, 2×10⁵ cells/well, and 4×10⁵ cells/well were transfected with FITC-DSP3.1 as described above. Controls included HeLa cells exposed to Lipofectamine™ 2000 alone and to media alone. The transfected cells were harvested after 24-48 hours and analyzed by a fluorescence-activated cell sorter (FACS). Transfection was more efficient at cell densities of 5×10⁴ cells/well or less.

[0163] Interference of DSP-3 expression by two different DSP-3 sequence specific siRNA polynucleotides, DSP3.1 (SEQ ID NO:______) and DSP3.2 (SEQ ID NO:______). Transfection of HeLa cells was performed as described for MKP-1. As controls, HeLa cells were transfected with non-specific MKP.1 (SEQ ID NO:______) and with transfection solution not containing the expression vector or siRNA.

[0164] Twenty-four hours after transfection, cell extracts were prepared either using RIPA buffer (see above) or 1% Triton X-100®. The extracts were analyzed by immunoblot (see above) using an anti-DSP-3 monoclonal antibody, clone 17, diluted 1:10,000 in TBST and binding was detected with HRP-conjugated anti-mouse IgG. DSP3.1 effectively decreased expression of DSP-3, whereas the level of expression in cells transfected with siRNA DSP3.2 was comparable to expression in the cells transfected with the non-specific MKP.1 siRNA. The cell extracts were also immunoblotted against an anti-PTP1B antibody, which demonstrated that protein expression of another protein expressed in the cells was not affected by the presence of siRNA polynucleotides. The data suggest that the decrease in the level of DSP-3 expression varies depending upon the particular sequence of the siRNA.

[0165] To evaluate the sensitivity of interference by specific siRNA polynucleotides, DSP3.1 siRNA (SEQ ID NO:______) was titrated in HeLa cells. HeLa cells were transfected as described above with DSP3.1 siRNA (SEQ ID NO:1) at a concentration of 1, 2, 5, 10, 20, and 100 nM. HeLa cells were also transfected at the same concentrations with non-specific siRNAs, cdc14a.1 (5′-caucgugcgaagguuccugtt-3′ (SEQ ID NO:6)) and CD45.2 (5′-gccgagaacaaaguggaugtt-3′ (SEQ ID NO:______)). An immunoblot of cell extracts prepared using RIPA buffer was probed with anti-DSP-3 monoclonal antibody clone 17. A second immunoblot was probed with an anti-JNK2 antibody. DSP-3 expression decreased to approximately the same level in cells transfected with 5, 10, 20, and 100 nM of the specific siRNA DSP3.1. The level of expression of DSP-3 also decreased in the presence of the lowest concentrations of siRNA DSP3.1 compared with DSP-3 expression in cells transfected with non-specific siRNAs. Expression of JNK2 was not affected.

[0166] The specificity of siRNA interference was demonstrated by co-transfecting HeLa cells with the DSP-3 expression vector and an siRNA, DSP3.3 (SEQ ID NO:______) that had two base differences from siDSP3.1. Transfection and immunoblotting were performed as described above for the titration experiment. The expression levels of DSP-3 polypeptide was effectively decreased in the presence of 1, 5, 10, 20, or 100 nM of DSP3.1 but not in cells transfected with DSP3.3. The level of expression of JNK2 was not affected.

EXAMPLE 2 Interference with Expression of Protein Tyrosine Phosphatases by Sequence-Specific Small Interfering RNA

[0167] This example describes RNA interference of transient and endogenous expression of various protein tyrosine phosphatases (PTPs).

[0168] Co-Transfection Assays to Determine Interference of PTP Expression by siRNA

[0169] DSP-11 and DSP-18

[0170] Interference of expression of FLAG®-tagged DSP-11 polypeptide and FLAG®-tagged DSP-18pr polypeptide (DSP-18) by sequence specific siRNA polynucleotides was determined. (FLAG® sequence: Asp-Tyr-Lys-Asp-Asp-Asp-Asp-Lys (SEQ ID NO:______)) (Sigma Aldrich, St. Louis, Mo.). Two siRNA sequences that were specific for DSP-11 polynucleotide (SEQ ID NO:______) encoding a DSP-11 polypeptide (SEQ ID NO:______) and two siRNA sequences specific for DSP-18pr polynucleotide (DSP-18, SEQ ID NO:______) encoding a DSP-18 polypeptide (SEQ ID NO:______) were designed using the criteria described in Example 1. The following sequences were used in the experiments.

[0171] DSP-11 Specific: DSP11.2: 5′-cuggcaccaugcuggccugtt-3′ [SEQ ID NO:   ] DSP11.4: 5′-agcagucuuccaguucuactt-3′ [SEQ ID NO:   ]

[0172] DSP-18 Specific: DSP18.2: 5′-cugccuugugcacugcuuutt-3′ [SEQ ID NO:   ] DSP18.4: 5′-gaguuuggcugggccaguutt-3′ [SEQ ID NO:   ]

[0173] Vectors for expression of DSP-18 and DSP-11 were prepared as follows. Vector pCMVTag2B (Stratagene, La Jolla, Calif.) was digested with restriction endonuclease BamHI (New England Biolabs, Beverly, Mass.) for 3 hours at 37° C. The digested vector was then incubated with Klenow polymerase (New England Biolabs) for 15 minutes at 25° C. to fill in the recessed 3′ termini, followed by an incubation of 30 minutes at 37° C. with calf intestinal phosphatase (New England Biolabs). The GATEWAY™ Reading Frame Cassette B (Invitrogen, Carlsbad, Calif.) was inserted into the pCMVTag2B vector by ligation with T4 DNA ligase (Invitrogen) overnight at 16° C. according to the supplier's instructions. DB3.1™ competent E. coli cells were transformed with the ligated vector (GWpCMVTag2), and DNA was isolated by standard molecular biology methods. DSP-11 and DSP-18 constructs were prepared by ligating a polynucleotide encoding DSP-11 (SEQ ID NO:25) and a polynucleotide encoding DSP-18 (SEQ ID NO:27) into a modified bacterial pGEX-6PKG expression vector (Amersham Biosciences), referred to as pGEX-6P1, according to standard methods known in the molecular biology art. DSP-11 and DSP18 constructs and the pENTR™ 1A entry vector (Invitrogen) were digested with EcoRI (New England Biolabs) for 3 hours at 37° C. The pENTR™ 1A clone was treated with calf intestinal phosphatase for 30 minutes at 37° C., and then DSP-11 and DSP-18 constructs were inserted into separate pENTR™ vectors by ligation overnight at 16° C. with T4 DNA ligase. Vector DNA was prepared from LIBRARY EFFICIENCY® DH5α™ cells (Invitrogen) that were transformed with each construct according to the supplier's recommendation.

[0174] FLAG® epitope-tagged DSP-11 and DSP-18 polypeptides were prepared by cloning the pENTR™ 1A-DSP-18 and substrate trapping mutant constructs into the GWpCMVTag2 vector. The pENTR™ 1A constructs containing the DSP-11 and the DSP-18 polynucleotides were linearized by digesting the constructs with Vsp I (Promega Corp., Madison, Wis.) for 2 hours at 37° C. The DNA was purified using a QIAGEN PCR Purification kit (QIAGEN, Inc., Valencia, Calif.), and 30 μl (100 ng/μl) was combined in a GATEWAY™ LR reaction with 6 μl linearized pENTR™ 1A-DSP-11, pENTR™ 1A-DSP-18, 3 μl TE buffer, 4 μl Clonase™ Enzyme, and 4 μl LR reaction buffer (Invitrogen) for 1 hour at room temperature. After addition of Proteinase K (Invitrogen) to each reaction for 10 minutes, LIBRARY EFFICIENCY® DH5α™ cells were transformed with each expression vector. For controls, FLAG®-DSP-3 and FLAG®-cdc14b were also prepared according to the above method.

[0175] 293-HEK cells, maintained in DMEM, 10% FBS at 37° C. and 5% CO₂, were co-transfected with the FLAG®-DSP-11, FLAG®-DSP-18, FLAG®-DSP-3, and FLAG®-cdc14b expression vectors and DSP11.2, DSP11.4, DSP18.2, and DSP18.4 siRNAs (20 nM) (double-stranded RNA was prepared as described in Example 1) using the Lipofectamine™ 2000 reagent (Invitrogen). After incubating the transfected cells for 22-24 hours at 37° C., cells were rinsed twice in phosphate buffered saline (PBS) (4° C.) and then lysed in 250 μl of ice-cold RIPA buffer (see Example 1). The cell debris was pelleted and aliquots of each supernatant were separated by SDS-PAGE and immunoblotted as described in Example 1. DSP-11 and DSP-18 polypeptides were detected by probing the immunoblots with an anti-FLAG® antibody (Sigma-Aldrich, St. Louis, Mo.) followed by probing with an HRP-conjugated goat anti-mouse reagent (see Example 1). Binding of the anti-FLAG® antibody was detected by chemiluminescence development (see Example 1). FIG. 2 shows that expression of FLAG®-DSP-11 and FLAG®-DSP-18 was inhibited in the presence of sequence-specific siRNA.

[0176] DSP-13 and DSP-14

[0177] Expression constructs of DSP-13 (SEQ ID NO:______) and DSP-14 (SEQ ID NO:______) and FLAG® epitope-tagged DSP-13 and DSP-14 polypeptides (SEQ ID NO:______ and SEQ ID NO:______, respectively) were prepared essentially as described above. Four siRNA sequences specific for DSP-13 polynucleotide and four siRNA sequences specific for DSP-14 were designed according to the criteria described in Example 1 except that melting temperatures were not necessarily calculated. After performing the BLAST search to analyze the specificity of a sequence, sequences that contained at least 16 consecutive nucleotides with 100% identity with a polynucleotide sequence other than the target sequence were not used in the experiments. The siRNA polynucleotides were manufactured by Dharmacon Research Inc. The sequences of the siRNA polynucleotides are as follows.

[0178] DSP-13 Specific: DSP13.1: 5′-cuugcgggaauucaaggaatt-3′ (SEQ ID NO:   ) DSP13.2: 5′-ccgagggguacgguauauctt-3′ (SEQ ID NO:   ) DSP13.3: 5′-caucaggcuggcuguaagatt-3′ (SEQ ID NO:   ) DSP13.4: 5′-cauggaucuaaaugccuugtt-3′ (SEQ ID NO:   )

[0179] DSP-14 Specific: DSP-14.1: 5′-gugaagacaagccucaagatt-3′ (SEQ ID NO:   ) DSP-14.2: 5′-gcucuacauuggcgaugagtt-3′ (SEQ ID NO:   ) DSP-14.3: 5′-gcgacgaccacaguaagautt-3′ (SEQ ID NO:   ) DSP-14.4: 5′-ggacaugacccugguggactt-3′ (SEQ ID NO:   )

[0180] 293-HEK cells were co-transfected with 1-2 μg of the FLAG®-DSP-13 or FLAG®-DSP-14 expression vector and 20 nM of siRNA and expression detected by immunoblot as described above. As controls, cells co-transfected with a DSP expression vector and a non-specific siRNA and untransfected 293-HEK cells were included in the analysis.

[0181] The amount of of FLAG®-DSP-13 polypeptide expressed in 293-HEK cells co-transfected with the FLAG®-DSP-13 construct and either DSP13.3 or DSP13.4 siRNA decreased more than 95% compared with cells transfected with the DSP-13 expression constructs only. Expression of the DSP-13 polypeptide in cells co-transfected with DSP13.2 siRNA was comparable to expression in cells co-transfected with a non-specific siRNA (DSP14.1). Expression of FLAG®-DSP-14 polypeptide decreased 70% in 293-HEK cells when the cells were co-transfected with DSP14.1 siRNA and decreased 90% when the cells were co-transfected with DSP-14.3 siRNA. Expression of DSP-14 in the presence of siRNA 14.4 was only slightly lower than observed with a non-specific siRNA (DSP13.1).

[0182] DSP-3

[0183] Transient co-transfection experiments in 293-HEK cells were also performed with DSP3.1 siRNA (SEQ ID NO:1) and a DSP-3 polypeptide recombinant expression vector (prepared according to standard molecular biology techniques). Expression of DSP-3 was determined by immunoblot probed with anti-DSP-3 monoclonal antibody clone 17. The results showed that the amount of DSP-3 polypeptide expressed in the 293-HEK cells decreased 80% in the presence of sequence specific siRNA.

[0184] SHP-2

[0185] Inhibition of expression of the protein tyrosine phosphatase (PTP) SHP-2 (src homology protein-2) was also examined in the 293-HEK co-transfection assay. Four different siRNAs specific for the polynucleotide sequence (SEQ ID NO:______) encoding SHP-2 (SEQ ID NO:______) were co-transfected with a FLAG®-SHP-2 expression construct prepared according to the molecular biology methods described above. SHP-2 specific siRNAs had the following sequences. SHP2.1: 5′-gauucagaacacuggugautt-3′ (SEQ ID NO:   ) SHP2.2: 5′-gaauauggcgucaugcgugtt-3′ (SEQ ID NO:   ) SHP2.3: 5′-cggucuggcaauaccacuutt-3′ (SEQ ID NO:   ) SHP2.4: 5′-ugacggcaagucuaaagugtt-3′ (SEQ ID NO:   )

[0186] The siRNA SHP2.1 effectively impaired expression of SHP-2 in transfected 293-HEK cells, decreasing the amount of FLAG®-SHP-2 polypeptide detected by more than 95%. In the presence of siRNA SHP2.2, FLAG®-SHP-2 polypeptide expression decreased by 85%. SHP2-4 had no specific effect on SHP-2 expression.

[0187] PRL-3 and KAP

[0188] Inhibition of expression of the human protein tyrosine phosphatases (PTP) PRL-3 and KAP were also examined in the 293-HEK co-transfection assay. Four different siRNAs specific for the polynucleotide sequence (SEQ ID NO:______) encoding PRL-3 (SEQ ID NO:______) were co-transfected with a FLAG®-PRL-3 expression construct prepared according to the molecular biology methods described above. Similarly, four different siRNAs specific for the polynucleotide sequence (SEQ ID NO:______) encoding KAP (SEQ ID NO:______) were co-transfected with a FLAG®-KAP expression construct. The siRNA sequences and the percent decrease in the level of expression of the PTP in cells transfected with the each siRNA is presented in Table 1 below, and it is noted that each 21-mer sequence below contains a dinucleotide “overhang” at the 3′ end, and that the invention herein should be considered to include the 19-mer polynucleotide sequences beginning at the 5′ end therein as well as the 21-mer polynucleotide shown in the Table. TABLE 1 siRNA INTERFERENCE WITH PRL-3 AND KAP IN CO-TRANSFECTION ASSAYS Related Decrease in Target siRNA Sequence (SEQ ID NO) siRNA Name SEQ ID NO: Expression KAP 5′-GAGCCUAUUGAAGAUGAACTT-3′ KAP.1  >90% KAP 5′-GAGCUGUGGUAUACAAGACTT-3′ KAP.2  >90% KAP 5′-GAGCUUACAACCUGCCUUATT-3′ KAP.3  >90% KAP 5′-UACACUGCUAUGGAGGACUTT-3′ KAP.4  <10% PRL-3 5′-GUGACCUAUGACAAAACGCTT-3′ Prl3.1  50% PRL-3 5′-GGCCAAGUUCUGUGAGGCCTT-3′ Prl3.2  50% PRL-3 5′-GUACGAGGACGCCAUCCAGTT-3′ Prl3.3  50% PRL-3 UACCGGCCCAAACAGAGGCTT Prl3.4 <10%

[0189] PTPε

[0190] Inhibition of expression of human PTPε is examined in the 293-HEK co-transfection assay. Four different siRNAs specific for the polynucleotide sequence (SEQ ID NO:______) encoding PTPε (SEQ ID NO:______) are co-transfected with a FLAG®-PTPε expression construct prepared according to the molecular biology methods described above. The siRNA sequences that are analyzed have AA leader sequences (not included in the siRNA polynucleotide transfected into HEK cells) and the following sequences. RPTPE.1: 5′GCAGAGGAAAGCUGUGGUCTT3′ (SEQ ID NO:   ) RPTPE.2: 5′GUCUGCGACCAUCGUCAUGTT3′ (SEQ ID NO:   ) RPTPE.3: 5′GCCUUACUCGAGUACUACCTT3′ (SEQ ID NO:   ) RPTPE.4: 5′GGACUAUUUCAUCGCCACCTT3′ (SEQ ID NO:   )

[0191] Interference by siRNA Polynucleotides of Endogenous PTP Expression

[0192] The effect of sequence specific siRNA polynucleotides on expression of protein tyrosine phosphatases endogenously expressed in cells was also determined. Inhibition of expression of SHP-2 in HeLa cells by specific siRNAs was examined. HeLa cells were transfected with 10 nM of SHP2.1 (SEQ ID NO:______); SHP2.2 (SEQ ID NO:______); DSP13.3 (SEQ ID NO:______); DSP14.1 (SEQ ID NO:______); and DSP14.3 (SEQ ID NO:______). Each siRNA was diluted in 50 μl OptiMEM® to provide a final concentration of 10 nM per well of cells in six well tissue culture plate. In a separate tube, 3 μl of Lipofectamine™ was combined with 10 μl OptiMEM®. Each solution was incubated for 7 minutes. The two solutions were then mixed and incubated at room temperature for 22 minutes. The final volume of the mixed solution was adjusted to 500 μl and then was added to the HeLa cells. Cells were transfected with the siRNAs or with annealing buffer alone. The transfected cells were incubated with siRNAs for 60 hours.

[0193] Cell lysates were prepared by extracting the cells in RIPA buffer as described in Example 1. The lysates were separated by SDS-PAGE gel and analyzed by immunoblot according to the procedures described in Examples 1 and above in Example 2 using an anti-SHP-2 murine monoclonal antibody (Santa Cruz Biotechnology, Inc., Santa Cruz, Calif.). The levels of expression of endogenous SHP-2 decreased by 75% in the presence of SHP2.2 and by 90% in the presence of SHP2.1. The expression of SHP-2 in the siRNAs presence of DSP13.3, DSP14.1, or DSP14.3 was comparable to the level of expression observed in cells treated with buffer only.

[0194] A similar experiment was performed to determine the level of endogenous expression of DSP-3 in HeLa cells and in MDA-MB-435 cells (ATCC) in the presence of sequence specific siRNA. DSP3.1 siRNA (SEQ ID NO:1) was transfected into each cell line as described above, and the level of expression of DSP-3 polypeptide was analyzed by immunoblot (see Example 1 for immunoblot procedure to detect DSP-3). Expression of DSP-3 polypeptide decreased 70-100% in HeLa cells and decreased 100% in MDA-MB-435 cells in the presence of the specific mRNA.

[0195] Particular siRNA polynucleotide sequences that are specific for CD45, SHP2, cdc14a, cdc14b, cdc25A, cdc25B, cdc25C, PRL-3, KAP, DSP-3, and PTPε are provided below. The level of expression of each PTP and DSP in cells that are capable of expressing the PTP or DSP and that are transfected with any one of the following specific siRNA polynucleotides is determined according to methods and procedures described above. The siRNA sequences that are incorporated into a vector from which a hairpin vector is transcribed and/or that are transfected via liposomes according to methods described in Examples 1 and 2 are presented in the following tables. The human TCPTP target sequences were derived from a human TCPTP nucleotide sequence (see GenBank Accession No. M25393, NM 002828, NM_(—)080422 (SEQ ID NOs:______)); the CD45 target sequences were derived from a human CD45 nucleotide sequence, (see Charbonneau et al. (SEQ ID NO:______)); the SHP-2 target sequences were derived from a human SHP-2 nucleotide sequence (see GenBank Accession No. L03535 and L07527 (SEQ ID NO:______)); the cdc14a target sequences were derived from a human cdc14a nucleotide sequence (see GenBank Accession No. AF122013 (SEQ ID NO:______)); the cdc14b target sequences were derived from a human cdc14b nucleotide sequence (GenBank Accession No. AF023158 (SEQ ID NO:______)); the cdc25A target sequences were derived from a human cdc25A nucleotide sequence (see GenBank Accession No. NM_(—)133571 and AF527417 (SEQ ID NO:______); the cdc25B target sequences were derived from a human cdc25B nucleotide sequence (see GenBank Accession No. M81934 (SEQ ID NO:______)); the cdc25C target sequences were derived from a human cdc25C nucleotide sequence (see GenBank Accession No. NM_(—)001790 (SEQ ID NO:______); the PRL-3 target sequences are derived from the human PRL-3 nucleotide sequence (see GenBank Accession No. NM_(—)032611 and NM_(—)003479 (SEQ ID NO:______); the KAP target sequences are derived from the human KAP nucleotide sequence (see GenBank Accession No. L2711 (SEQ ID NO:______)); the DSP-3 target sequences were derived from the human DSP-3 nucleotide sequence set forth in (SEQ ID NO:778); and the PTPε target sequences were derived from the human PTPε nucleotide sequence (see GenBank Accession No. NM_(—)006504 and NM_(—)130435 (SEQ ID NO:______)).

[0196] siRNA polynucleotide sequences were selected using the Dharmacon siDESIGN system (Dharmacon Research). These sequences were generated using the following parameters: (1) leader sequences included dinucleotides AA, CA, TA, and GA; (2) the coding region (CR) was scanned; (4) the G+C content varied from approximately 31-63%; (5) overlaps of sequences within different 19 nucleotide sequences were permitted. These sequences were then compared to known human genome sequences using the BLAST program. Potential target sequences were eliminated if 16 or more consecutive nucleotides within the 19-nucleotide target sequence were identified in another human polynucleotide sequence. The remaining 19-nucleotide siRNA sequences are presented in the tables below. Each siRNA sequence represented in Tables 2-12 lists the sequence of the sense strand of the siRNA and its corresponding sequence identifier. For PRL-3, only one sequence (AGACCCGGUGCUGCGUUAU, SEQ ID NO:______) was identified by this method. An siRNA polynucleotide as described herein is understood to be composed of the 19 nucleotide sense strand and its complementary (or antisense) strand. In addition, a siRNA polynucleotide of the present invention typically has a dinucleotide overhang at the 3′ end of each strand, which may be any two nucleotides. Accordingly, it is noted that each 21-mer sequence below contains a dinucleotide “overhang” at the 3′ end, and that the invention herein should be considered to include the 19-mer polynucleotide sequences beginning at the 5′ end therein as well as the 21-mer polynucleotide shown in the Tables. TABLE 2 HUMAN CD45 siRNA POLYNCULEOTIDE SEQUENCES (POST-BLAST) 19-Nucleotide Target Sequence Region SEQ ID NO. CCACCAUCACAGCGAACAC CR AGCGCUGUCAUUUCAACCA CR ACCACAACAAUAGCUACUA CR GCUACUACUCCAUCUAAGC CR AAUGCGUCUGUUUCCAUAU CR AUGCGUCUGUUUCCAUAUC CR UGCGUCUGUUUCCAUAUCU CR ACCUUUACUUGUGAUACAC CR CAGAUUUCAGUGUGGUAAU CR ACCCGAACAUGAGUAUAAG CR CCCGAACAUGAGUAUAAGU CR CAAGUUUACUAACGCAAGU CR GGAGUAAUUACCUGGAAUC CR CAUGCCUACAUCAUUGCAA CR AUAGUAUGCAUGUCAAGUG CR UGAACGUUACCAUUUGGAA CR AUGAGUCGCAUAAGAAUUG CR UGAGUCGCAUAAGAAUUGC CR GAAUUGCGAUUUCCGUGUA CR AUUGCGAUUUCCGUGUAAA CR GCCAAUCCAUGCAGAUAUU CR UUAUAACCGUGUUGAACUC CR UAACCGUGUUGAACUCUCU CR ACGGAGAUGCAGGGUCAAA CR GAUGCAGGGUCAAACUACA CR ACCCAGGAAAUACAUUGCU CR UGUCCAGAUUACAUCAUUC CR AUGCCUUCAGCAAUUUCUU CR CAGGAACCUAUAUCGGAAU CR GGAACCUAUAUCGGAAUUG CR ACCUAUAUCGGAAUUGAUG CR GUGGAUGUUUAUGGUUAUG CR GGCGACAGAGAUGCCUGAU CR GAGGCCCAGUACAUCUUGA CR GGCCCAGUACAUCUUGAUC CR GCUACUGGAAACCUGAAGU CR ACCUGAAGUGAUGAUUGCU CR AGUUGACCUGAAAGACACA CR ACUUAUACCCUUCGUGUCU CR CUUAUACCCUUCGUGUCUU CR GGAAAGACUCUCGAACUGU CR ACCCAAGGAAUUAAUCUCU CR CCCAAGGAAUUAAUCUCUA CR UGAUUCAGGUCGUCAAACA CR GGGAUGGAUCUCAGCAAAC CR UCUCAGCAAACGGGAAUAU CR UUCGAGCAAUAUCAAUUCC CR CCUACCCUGCUCAGAAUGG CR

[0197] TABLE 3 HUMAN SHP-2 siRNA POLYNCULEOTIDE SEQUENCES (POST-BLAST) 19-Nucleotide Target Sequence Region SEQ ID NO. AUGGAGCUGUCACCCACAU CR UGGAACAUCACGGGCAAUU CR GCAAUGACGGCAAGUCUAA CR AUGACGGCAAGUCUAAAGU CR UGACGGCAAGUCUAAAGUG CR GUCUAAAGUGACCCAUGUU CR UGAUUCGCUGUCAGGAACU CR CGACGUUGGUGGAGGAGAA CR ACGGUUUGAUUCUUUGACA CR UUCUUUGACAGAUCUUGUG CR GAAUCCUAUGGUGGAAACA CR AUCCUAUGGUGGAAACAUU CR UCCUAUGGUGGAAACAUUG CR CAGUACUACAACUCAAGCA CR UUUGAGACACUACAACAAC CR AACUUCUCUACAGCCGAAA CR ACAUCCUGCCCUUUGAUCA CR UCAUACCAGGGUUGUCCUA CR UACCAGGGUUGUCCUACAC CR UUUGAAACCAAGUGCAACA CR AGAGUUACAUUGCCACACA CR GAGUUACAUUGCCACACAA CR AAACACGGUGAAUGACUUU CR CUGGCCUGAUGAGUAUGCU CR UGGCGUCAUGCGUGUUAGG CR UGCGUGUUAGGAACGUCAA CR UGACUAUACGCUAAGAGAA CR CUAUACGCUAAGAGAACUU CR GGUUGGACAAGGGAAUACG CR GAACGGUCUGGCAAUACCA CR CGGUCUGGCAAUACCACUU CR AAGGUGUUGACUGCGAUAU CR AGGUGUUGACUGCGAUAUU CR GGUGUUGACUGCGAUAUUG CR UAUGGCGGUCCAGCAUUAU CR UGGCGGUCCAGCAUUAUAU CR AACACUACAGCGCAGGAUU CR ACACUACAGCGCAGGAUUG CR GCGCAGGAUUGAAGAAGAG CR GAGGAAAGGGCACGAAUAU CR GGAAAGGGCACGAAUAUAC CR GGGCACGAAUAUACAAAUA CR AAACGUGGGCCUGAUGCAA CR ACGUGGGCCUGAUGCAACA CR

[0198] TABLE 4 HUMAN CDC14A siRNA POLYNCULEOTIDE SEQUENCES (POST-BLAST) 19-Nucleotide Target Sequence Region SEQ ID NO. GCACAGUAAAUACCCACUA CR CUAUUUCUCCAUCGAUGAG CR ACUUGGCAAUGGUGUACAG CR GGUGCCUAUGCAGUAAUCU CR UCUCACCAUUCUCGACUGU CR AAGGGAUUACAACAUGGAU CR AGGGAUUACAACAUGGAUU CR GGGAUUACAACAUGGAUUU CR GAAUGGUUAUCCUCUUCAC CR GCAUAAUGUGACUGCAGUU CR CGCUGGCUUCGAGCACUAU CR GCACACCCAGUGACAACAU CR ACAUCGUGCGAAGGUUCCU CR AGAACAGGGACAUUGAUAG CR GAACAGGGACAUUGAUAGC CR GGGACAUUGAUAGCCUGUU CR CAUUGAUAGCCUGUUAUGU CR CUACAGGUUUACACAUGCU CR AAAUCGACCAUCCAGUGAA CR AAUCGACCAUCCAGUGAAG CR UCGACCAUCCAGUGAAGGA CR AAAUUCUUUCUGGCCUAGA CR UGUCUAUUGGUGGAAAUCU CR ACGAUUUGGAGAGGUAAGU CR CGAUUUGGAGAGGUAAGUU CR

[0199] TABLE 5 HUMAN CDC14B siRNA POLYNCULEOTIDE SEQUENCES (POST-BLAST) 19-Nucteotide Target Sequence Region SEQ ID NO. GAGACAUCCUAUAUUCCUU CR AUACCAGACCGAUUUAUUG CR UACCAGACCGAUUUAUUGC CR GACCGAUUUAUUGCCUUCU CR AAGGAUGUAUGAUGCCAAA CR AGGAUGUAUGAUGCCAAAC CR GGAUGUAUGAUGCCAAACG CR CGGAUGCUGGCUUCGAUCA CR UGCCAUUGUCAAAGAAUUC CR GGGUGCCAUUGCAGUACAU CR GACCUGGCUCGGUGAUUGG CR CCCGAACCGUACAGUGAUG CR ACCGUACAGUGAUGAUGAC CR UAGACUUCGGGCCUUGAAA CR ACAAACGCUAUUCCUCUCA CR

[0200] TABLE 6 HUMAN CDC25A siRNA POLYNCULEOTIDE SEQUENCES (POST-BLAST) 19-Nucleotide Target Sequence Region SEQ ID NO. GGGUCUGGGCAGUGAUUAU CR GCAACCACUGGAGGUGAAG CR AUCCUAUGAGAAGAAUACA CR UCCUAUGAGAAGAAUACAU CR AAAGCUGUUGGGAUGUAGU CR UUCUGAUUCUCUUGACCAU CR GAAGCCAGUAAGACCUGUA CR CAGCCACUUUGUCUGAUGA CR AACCUUGACAACCGAUGCA CR CAACCGAUGCAAGCUGUUU CR ACCGAUGCAAGCUGUUUGA CR CUCGGUCAGUGUUGAAGAG CR ACGUUCUCAAGAGGAGUCU CR GUCAACUAAUCCAGAGAAG CR AGGCCCAUGAGACUCUUCA CR AGGGACCUUAUAGGAGACU CR GGGACCUUAUAGGAGACUU CR GACUUCUCCAAGGGUUAUC CR GUUUGUUAUCAUCGACUGU CR CUGUCGAUACCCAUAUGAA CR GAAGCCCAUUGUACCUACU CR AGCCCAUUGUACCUACUGA CR GCCCAUUGUACCUACUGAU CR UGGCAAGCGUGUCAUUGUU CR AGCGUGUCAUUGUUGUGUU CR UGUGCCGGUAUGUGAGAGA CR GAGAGAUCGCCUGGGUAAU CR GAGAUCGCCUGGGUAAUGA CR GAUCGCCUGGGUAAUGAAU CR

[0201] TABLE 7 HUMAN CDC25B siRNA POLYNCULEOTIDE SEQUENCES (POST-BLAST) 19-Nucleotide Target Sequence Region SEQ ID NO. AUCCUCCCUGUCGUCUGAA CR UCCUCCCUGUCGUCUGAAU CR UGGCGGAGCAGACGUUUGA CR CGUUUGAACAGGCCAUCCA CR GCCGGAUCAUUCGAAACGA CR UCAUUCGAAACGAGCAGUU CR GUCUAUGCCGGAUGGAUUU CR UGCCGGAUGGAUUUGUCUU CR AAAGGACCUCGUCAUGUAC CR AAUCACUGUGUCACGAUGA CR AUCACUGUGUCACGAUGAG CR GAGCUGAUUGGAGAUUACU CR GCUGAUUGGAGAUUACUCU CR CUCUAAGGCCUUCCUCCUA CR CAGACAGUAGACGGAAAGC CR AGCACCAAGACCUCAAGUA CR GAAACGAUGGUGGCCCUAU CR AACGAUGGUGGCCCUAUUG CR CGCCGAGAGCUUCCUACUG CR

[0202] TABLE 8 HUMAN CDC25C siRNA POLYNCULEOTIDE SEQUENCES (POST-BLAST) 19-Nucleotide Target Sequence Region SEQ ID NO. GAACUCCAGUGGGCAAAUU CR UUUAGCUGGGAUGACAAUG CR UUCAAGGACAACACAAUAC CR ACACAAUACCAGAUAAAGU CR CACAAUACCAGAUAAAGUU CR GGAAGGGCUUAUGUUUAAA CR CACCAAGAUCUGAAGUAUG CR AGUAUGUCAACCCAGAAAC CR GUAUGUCAACCCAGAAACA CR UGUCAUUGAUUGUCGCUAU CR UUGAUUGUCGCUAUCCAUA CR UUGUCGCUAUCCAUAUGAG CR UCCAGGGAGCCUUAAACUU CR GGGAGCCUUAAACUUAUAU CR GUCAGGAAGAACUGUUUAA CR AGAAGCCCAUCGUCCCUUU CR GAAGCCCAUCGUCCCUUUG CR AGCCCAUCGUCCCUUUGGA CR CACCCAGAAGAGAAUAAUC CR UUGUACUACCCAGAGCUAU CR CUACCCAGAGCUAUAUAUC CR CCCAGAGCUAUAUAUCCUU CR UAUAUGGAACUGUGUGAAC CR UAUGGAACUGUGUGAACCA CR CAGAGCUACUGCCCUAUGC CR GAGCUACUGCCCUAUGCAU CR GCUACUGCCCUAUGCAUCA CR

[0203] TABLE 9 HUMAN KAP siRNA POLYNCULEOTIDE SEQUENCES (POST-BLAST) 19-Nucleotide Target Sequence Region SEQ ID NO. GAUGAAGAGCCUAUUGAAG CR AGAUGAACAGACUCCAAUU CR GAUGAACAGACUCCAAUUC CR UCACCCAUCAUCAUCCAAU CR GAGCUUACAACCUGCCUUA CR CACUGCUAUGGAGGACUUG CR UCACCAGAGCAAGCCAUAG CR CCAGAGCAAGCCAUAGACA CR CAGCCUGCGAGACCUAAGA CR GUUUCGGGACAAAUUAGCU CR AAUUAGCUGCACAUCUAUC CR AUUAGCUGCACAUCUAUCA CR UUAGCUGCACAUCUAUCAU CR

[0204] TABLE 10 HUMAN DSP-3 siRNA POLYNCULEOTIDE SEQUENCES (POST-BLAST) 19-Nucleotide Target Sequence Region SEQ ID NO. GAGACGCGGAACAAUUGAG CR AGAACAAGGUGACACAUAU CR GAACAAGGUGACACAUAUU CR GCAGCGGAUUCACCAUCUC CR GCGGAUUCACCAUCUCAAA CR CACUGGUGAUCGCAUACAU CR GUAUCGGCAGUGGCUGAAG CR

[0205] TABLE 11 HUMAN PTP EPSILON siRNA POLYNCULEOTIDE SEQUENCES (POST-BLAST) 19-Nucleotide Target Sequence Region SEQ ID NO. GAUCCGCCGACGACUGCAA CR GUUUCGGGAGGAGUUCAAC CR AUGACCAUUCUAGGGUGAU CR CCAUUCUAGGGUGAUUCUG CR CAUAGAUGGUUACAAAGAG CR AACAGGAAACGGUUAACGA CR GGAAACGGUUAACGACUUC CR CCAUCGUCAUGUUAACAAA CR CUACACCAUCCGGAAGUUC CR UCCGGAAGUUCUGCAUACA CR GAAAGUAAAGACGCUCAAC CR GCGCCCUCAGAUGGUUCAA CR CGGAUAUGCAGUACACGUU CR CCACCCACUUCGACAAGAU CR CAAAUGUCCGGAUCAUGAA CR CAUGAGGACGGGCAACUUG CR UGACUUCAACCGAGUGAUC CR ACCGAGUGAUCCUUUCCAU CR AGAAUACACAGACUACAUC CR GACUACAUCAACGCAUCCU CR UCAACGCAUCCUUCAUAGA CR CACACGGUUGAGGACUUCU CR AAUCCCACACUAUCGUGAU CR AUCCCACACUAUCGUGAUG CR ACCGAGGGCUCAGUUACUC CR CCGAGGGCUCAGUUACUCA CR CUCAUGGAGAAAUAACGAU CR UGGAGAAAUAACGAUUGAG CR GCCAUCAGUAUACGAGACU CR UCAGUAUACGAGACUUUCU CR GGGCAAAGGCAUGAUUGAC CR GCUGGGCGAACAGGUACAU CR CUUCAGAGACCACAUAUGG CR

EXAMPLE 3 Decreased Activation of JNK in the Presence of siRNA Specific for DSP-3

[0206] This Example describes the effect on JNK activation by sequence-specific siRNA interference of DSP-3 polypeptide expression.

[0207] HeLa cells were transfected with 60 pmoles of DSP3.1 siRNA (SEQ ID NO:1) or 60 pmoles CD45.2 (SEQ ID NO:13) as described in Example 1. After the incubation following transfection, cells were stimulated with 10 ng/ml TNF-α or 10 ng/ml EGF for 10 minutes or with 500 mM sorbitol for 30 minutes, which are known stimulators of the JNK signal transduction pathway (WO 01/21812; Shen et al. Proc. Natl. Acad. Sci. 98:13613-18 (2001)). After the stimulators were decanted, the 6-well plate of cells was frozen. The cells were treated with 0.5 ml Extraction Buffer (20 mM Tris, pH 8, 136 mM NaCl, 50 mM NaF; 1 mM V04; 0.2 mM EDTA, 0.2 mM EGTA, 20 nM Calyculin, 10% glycerol, 0.5% nonidet P40, 1 μg/ml of aprotinin, pepstatin, and leupeptin; and 1 mM Benzamidine) (4° C.). When the cells had partially thawed, the wells of the plates were scraped and the cells were collected. The wells were washed 3× with Extraction Buffer and the washes were combined with the cells. After centrifugation of the extracted cells, the supernatants were decanted. The protein concentration of each extract was determined by the Bradford protein assay. Volumes of the different extracts were adjusted with Extraction Buffer to the concentration of the extract having the lowest protein concentration.

[0208] JUN, a substrate of JNK, conjugated to glutathione (GSH) (GST-cJUN) (Shen et al., supra) in 20 mM Tris, pH 7.2, 1 nM EDTA, and 150 mM NaCl was combined with 200-250 μl of Glutathione-Sepharose (Amersham Biosciences, Piscataway, N.J.). After mixing for 45 minutes at 4° C., the conjugated sepharose beads were washed twice in Extraction Buffer and then resuspended in 1 ml of Extraction Buffer.

[0209] cJUN-Sepharose (20 μl) was added to each cell extract sample. The mixtures were gently mixed for 2 hours at 4° C., followed by one wash in 1 ml Extraction Buffer and once in 1 ml kinase buffer (20 mM Pipes, pH 7.2, 10 mM MgCl₂, 1 mM DTT, 0.1% Triton X-100, and 1 MM sodium vanadate). The mixtures were centrifuged and the pellets were kept on ice. ATP mix (300° C./ml of [γ-³²P]ATP (3000 Ci/mmole) in kinase buffer) was incubated in a heat block to bring the solution to 30° C. ATP mix (15 μl) was added to each cold cJUN-Sepharose pellet at time intervals of 20 seconds. After the ATP mix was added, each sample was vortexed gently for 5 seconds and then placed in the 30° C. heat block. Each sample was gently mixed again for 5 seconds at 20-second intervals. After 20 minutes, the reactions were stopped at 20-second intervals with 15 μl 2×SDS-PAGE sample buffer. The samples were immediately heated at 100° C. for 5 minutes, then mixed and frozen at −20° C. The extracts were thawed and applied to 8-16% NOVEX® gels. After electrophoresis, the gels were dried and the cJUN band was cut from the gel and the radioactivity was counted (Cerenkov measurement). As shown in FIGS. 3 and 4, JNK activation as measured by the presence of phosphorylated JUN was mediated less by cells transfected with siRNA specific for DSP-3 than in cells transfected with a non-specific siRNA.

[0210] Because EGF induces a signaling pathway involving the ERK MAP kinase family, the effect on ERK phosphorylation in HeLa cells transfected with DSP-3 specific siRNA was determined. Transfection of HeLa cells and stimulation of the JNK signaling pathway was performed as in the previous experiment. Additional transfected cell cultures were stimulated with anisomycin. Phosphorylation of ERK was determined in a similar manner as described above for cJUN except that after electrophoresis of the cell extract samples, the proteins separated in the gel were transferred to a PVDF membrane. The immunoblot was probed with an anti-phospho-ERK antibody (1:1000) followed by incubation with the appropriate HRP-conjugated reagent and detection by chemiluminescence. As shown in FIG. 5, phosphorylation of ERK induced by stimulation of the cells with EGF and sorbitol was not affected by interference of DSP-3 polypeptide expression by specific siRNA DSP3.1.

EXAMPLE 4 Interference of Expression and Function of Cell Division Cycle Proteins by Specific siRNA

[0211] This example describes interference of expression of cell division cycle (cdc) proteins, cdc14a, cdc14b, and cdc25A, cdc25B, and cdc25C polypeptides by sequence specific siRNA polynucleotides. The effect on the function of these polypeptides in the presence of siRNA was also determined.

[0212] Interference with Cell Division Cycle Protein Expression by Specific siRNA

[0213] Two siRNA sequences that were specific for cdc14a polynucleotide (SEQ ID NO:33) encoding a cdc14a polypeptide (SEQ ID NO: 34) and two siRNA sequences specific for cdc14b polynucleotide (SEQ ID NO:35) encoding a cdc14b polypeptide (SEQ ID NO:36) were designed using the criteria described in Example 1. Recombinant expression vectors containing polynucleotide sequences encoding FLAG®-tagged cdc14a polypeptide and FLAG®-tagged cdc14b polypeptide were prepared essentially according to methods described in Example 2 with the following exceptions. 293-HEK cells were cultured in 35 mm culture dishes and were transfected with FLAG vectors at a concentration of 1 μg per well. 293-HEK cells were co-transfected with FLAG®-tagged cdc14a expression vector and the following siRNAs at 20 nM per well: cdc14a.2 (5′-caucugugagaacaccgaatt-3′, SEQ ID NO:______); cdc14a.3 (5′-cuuggcaaugguguacagatt-3′, SEQ ID NO:______); cdc14a.4, SEQ ID NO:______), cdc14a.5 (5′-gcacaguaaauacccacuatt-3′, SEQ ID NO:______); DSP3.1 (SEQ ID NO:______); DSP3.2 (SEQ ID NO:______); cdc14b.3 (5′-caagcaaaugcugccuucctt-3′, SEQ ID NO:______); cdc14b.4 (5′-gagccagacuugaaaguggtt-3′, SEQ ID NO:______); MKP.2 (SEQ ID NO:______); and CD45.3 (negative control). Controls included 293-HEK cells that were not transfected with any vector or siRNA and 293-HEK cells transfected with FLAG®-tagged cdc14a in the presence of siRNA annealing buffer. The level of expression in each sample was analyzed by immunoblot as described in Example 2 using an anti-FLAG® antibody. As shown in FIG. 6, specific siRNAs, cdc14a.2, cdc14a.3, and cdc14a.5 interfered with expression of cdc14a polypeptide most effectively.

[0214] Specificity of cdc14a.3 siRNA for interfering with expression of cdc14a and not other dual specificity phosphatases was shown by co-transfecting cdc14a.3 siRNA with FLAG®-tagged cdc14a (1 μg per 35 mm well of cells), FLAG®-tagged DSP-3, FLAG®tagged cdc14b, and FLAG®-tagged DSP-11. A FLAG® recombinant expression construct containing a polynucleotide sequence (SEQ ID NO:______) encoding a DSP-3 polypeptide (SEQ ID NO:______) was prepared as described for constructing other FLAG vectors. 293-HEK cell transfections and analysis of polypeptide expression levels were performed as described in Example 2. FIG. 7 shows that siRNA cdc14a.3 interfered with expression of only the cdc14a dual specificity phosphatase.

[0215] 293-HEK cells were co-transfected with FLAG®-tagged cdc14b expression vector (2 μg/35 mm well) and the following siRNAs at 20 nM per well: cdc14b.3 (SEQ ID NO:______); cdc14b.4 (SEQ ID NO:______); cdc14a.3 (SEQ ID NO:______)); cdc14a.5 (SEQ ID NO:______)); DSP3.1 (SEQ ID NO:______); DSP3.2 (SEQ ID NO:______); MKP.2 (SEQ ID NO:______); and CD45.3. Controls included 293-HEK cells that were not transfected with any vector or siRNA and 293-HEK cells transfected with FLAG®-tagged cdc14b in the presence of siRNA annealing buffer. The level of expression in each sample was analyzed by immunoblot as described in Example 2 using an anti-FLAG® antibody. As shown in FIG. 8, only specific siRNAs, cdc14b.3 and cdc14b.4 interfered with expression of cdc14b polypeptide.

[0216] Specificity of cdc14b.3 and cdc14b.4 siRNAs for interfering with expression of cdc14b and not other dual specificity phosphatases was shown by co-transfecting the siRNAs with FLAG®-tagged cdc14b (2 μg per 35 mm well), FLAG®-tagged DSP-3, and FLAG®-tagged DSP-11. Cells transfected with FLAG®-tagged DSP-3 and FLAG®-tagged DSP-11 were also co-transfected with cdc14a.5 siRNA. 293-HEK cell transfections and analysis of polypeptide expression levels were performed as described in Example 2. FIG. 9 shows that cdc14b.3 and cdc14b.4 siRNAs interfered with expression of only the cdc14b dual specificity phosphatase.

[0217] Expression of cdc14b polypeptide co-transfected with cdc14b.4 siRNA in HeLa cells was analyzed by immunocytochemistry. HeLa cells were co-transfected with a cdc14b recombinant expression vector and siRNA. Expression of cdc14b was detected by standard immunocytochemistry methods. As shown in FIG. 10, cdc14b.4 siRNA interfered with expression of cdc 14b polypeptide (top and bottom right panels).

[0218] The efficacy of RNAi against FLAG®-tagged Cdc25A expression in 293-HEK cells was also determined. Cells were co-transfected with a FLAG®-Cdc25A expression construct (prepared as described in Example 2) and specific siRNAs 25A.1, 25A.2, 25A.3, and 25A.4 (20 nM) and non-specific siRNAs (25B.1-0.4 and 25C.1-0.4). The level of expression of Cdc25A was determined by immunoblotting with an anti-FLAG® antibody. Only siRNA 25A.2 (5′-gaggagccauucugauucutt-3′ (SEQ ID NO:______)) effectively inhibited expression of Cdc25A.

[0219] The effect of RNAi on endogenous expression of Cdc25B and Cdc25C was examined in HeLa cells. The experiments were performed essentially as described in Example 2, except that HeLa cells were exposed to 10 nM siRNA polynucleotides for 48 hours. Four siRNAs specific for Cdc25A: 25A.1, 25A.2, 25A.3, and 25A.4 (20 nM); four siRNAs specific for Cdc25B: 25B.1, 25B.2, 25B.3, and 25B.4 (20 nM); and four siRNAs specific for Cdc25C: 25C.1, 25C.2, 25C.3, and 25C.4 (20 nM) were transfected into HeLa cells and expression was analyzed by immunoblotting cell lysates separated by SDS-PAGE using a Cdc25B antibody (Santa Cruz Biotechnololgy, Cat. No. c-20) and a Cdc25C antibody (Santa Cruz Biotechnololgy, Cat. No. h-85). The level of expression of Cdc25B was decreased 40-50% in HeLa cells transfected with siRNA cdc25B.2 (5′-aggcggcuacaaggaguuctt-3′ (SEQ ID NO:______)), and 50-60% in cells transfected with cdc25B.4 siRNA 5′-gaugccauggaagcccacatt-3′ (SEQ ID NO:______)). In HeLa cells transfected with siRNAs specific for Cdc25C, the level of expression of Cdc25C decreased 90% in HeLa cells transfected with cdc25C.1 (5′-cugccacucagcuuaccactt-3′ (SEQ ID NO:______)); decreased 70-80% in cells transfected with cdc25C.3 (5′-cccagaaacaguggcugcctt-3′ (SEQ ID NO:______)); and decreased 70-80% in cells transfected with Cdc25C.4 (5′-aggcggcuacagagacuuctt-3′ (SEQ ID NO:______)).

[0220] The ability of cancer cell lines to mediate RNA interference was examined by co-transfecting several cancer cell lines with a FLAG® cdc14b expression construct and specific siRNAs. The cell lines included SW620 (colon cancer); MCF7 (breast cancer); HS578T (breast cancer); MDA MB 231 (breast cancer); and T47D (breast cancer) (ATCC, NCI 60 panel). The FLAG® cdc14b expression construct (1−2 μg) was co-transfected with 20 nM of 14b.3 siRNA (SEQ ID NO:______); 14b.4 siRNA (SEQ ID NO:______); or MKP.2 siRNA (SEQ ID NO:______) (non-specific control) into each cell line as described in Example 2. The level of expression was analyzed by immunoblotting with an anti-FLAG® antibody according to the method described in Example 2. Expression of cdc14b was decreased in each of the five cell lines that were co-transfected with a cdc14b specific siRNA polynucleotide.

[0221] Effect of CDC-Specific siRNA on Cell Proliferation

[0222] Proliferation of cancer cells in the presence of siRNA polynucleotides specific for cdc14a, cdc14b, and Cdc25A, Cdc25B, and Cdc25C was determined. Cell proliferation was assessed according to a quantitative metabolic assay that measures the enzymatic conversion by cellular dehydrogenase in viable cells of a yellow tetrazolium salt (methylthiazoletetrazolium (MTT)) to purple formazan crystals. MDA-MB-231, SW620, and HeLa cell lines were transfected according to the procedures described in Examples 1 and 2 with the following siRNA polynucleotides (5 nM): cdc14a.3 (5′-cuuggcaaugguguacagatt-3′ (SEQ ID NO:______)); cdc14a.5 (5′-gcacaguaaauacccacuatt-3′ (SEQ ID NO:______)); cdc14b.3 (5′-caagcaaaugcugccuucctt-3′ SEQ ID NO:______); cdc14b.4 (5′-gagccagacuugaaaguggtt-3′ SEQ ID NO:______); cdc25A.2 (SEQ ID NO:______); cdc25B.4 (SEQ ID NO:______); cdc25C.1 (SEQ ID NO:______). The transfected cells were seeded at in a tissue culture plate and maintained for 5 days. A MTT assay was performed according to manufacturer's instructions (ATCC MTT Cell Proliferation Assay Kit, Cat. NO. 30-1010K, ATCC). The MTT-containing media was removed from the wells and was added to solubilize the formazan. The amount of formazan formed was determined by measuring absorbance at 570 m. Compared to the buffer only control, a significant decrease in proliferation was observed in MDA-MB-231 cells transfected with cdc14a.3, cdc14a.5, cdc14b.3, cdc14b.4, and cdc25B.4, and in HeLa cells transfected with cdc14a.3, cdc14a.5, cdc14b.4, and cdc25B.4. A significant decrease in cell proliferation of SW620 cells transfected with cdc14a.3 or cdc14a.5 was also observed.

[0223] Effect of CDC-Specific siRNA on Proapoptotic Signaling

[0224] Poly(ADP-ribose) polymerase (PARP) is a nuclear DNA binding protein that participates in genome repair, DNA replication, and the regulation of transcription. Cleavage of PARP (approximately 115 kDa) by members of the caspase family into polypeptide fragments of approximately 85 kDa and 25 kDa prevents PARP from performing its normal repair functions and appears to be an early event in apoptotic cell death. The cleaved PARP fragments can be detected by a variety of immunodetection methods.

[0225] HeLa cells were transfected with cdc14a.5 (SEQ ID NO:______); cdc14b.4 (SEQ ID NO:______); cdc25A.2 (SEQ ID NO:______); cdc25B.4 (SEQ ID NO:______); and cdc25C.1 (SEQ ID NO:______) at a concentration of 10 nM. After incubating the transfected cells for at 37° C., cell lysates were prepared and an immunoblot performed an antibody that that specifically binds to cleaved PARP and an antibody that binds to PARP (Cell Signaling Technology, Beverly, Mass.). The results are presented in FIG. 24. The data indicated that inhibiting expression of cdc14a by specific siRNA induces proapoptotic signaling to a greater extent than inhibition of expression of the other cell division cycle proteins.

EXAMPLE 5 Interference of PTP-1B and TC-PTP Expression by Specific siRNA

[0226] This Example describes interference with expression of two protein tyrosine phosphatases, PTP-1B and TC-PTP, using sequence specific siRNA polynucleotides.

[0227] Interference of Endogenous Expression of Murine PTP-1B in Mouse Fibroblasts by Sequence Specific siRNA Polynucleotides

[0228] Three siRNA sequences that were specific for murine PTP-1B polynucleotide (GenBank Acc. No. NM_(—)011201, SEQ ID NO:______) encoding a murine PTP-1B polypeptide (GenBank Acc. No. NM_(—)011201, SEQ ID NO:______) and one siRNA sequences specific for human PTP-1B polynucleotide (GenBank Ace. No. NM_(—)02827, SEQ ID NO:______) encoding a human PTP-1B polypeptide (GenBank Ace. No. NM_(—)02827, SEQ ID NO:______) were designed using the criteria described in Examples 1 and 2. Mouse C57B16 #3 cells, clones 3 and 10, were maintained in cell culture according to standard cell culture methods. Each C57B16 #3 clone was transfected with 200 nM of the following siRNAs: mPTP1B.1 (SEQ ID NO:______), mPTP1B.2 (SEQ ID NO:______), mPTP1B.3 (SEQ ID NO:______), and hPTP1B.1 (SEQ ID NO:______). Each siRNA was diluted in 50 μl O_(PTI)MEM® to provide a final concentration of 200 nM per well. In a separate tube, 3 μl of Lipofectamine™ was combined with 10 μl O_(PTI)MEM®. Each solution was incubated for 7 minutes. The two solutions were then mixed and incubated at room temperature for 22 minutes. The final volume of the mixed solution was adjusted to 100 μl and then the C57B16 #3 cells were added. Cells were transfected with the specific siRNAs, the human PTP1B siRNA, or annealing buffer alone. The transfected cells were incubated with siRNAs for six days.

[0229] Cell lysates were prepared by extracting the cells in ELISA extraction buffer (50 mM Tris-HCl, pH 7.5 (room temperature); 2 mM EDTA, pH 7-8; 1 mM phosphate (polyphosphate); 1 mM NaVO4 (monomeric), pH 10; 0.1% Triton X-100; Protease Inhibitor Cocktail set III, (Calbiochem, San Diego, Calif., catalog #539134)). The lysates were separated by SDS-PAGE gel and analyzed by immunoblot according to the procedures described in Examples 1 and 2 using an anti-PTP1B murine monoclonal antibody (Dr. Ben Neel, Harvard University, Cambridge, Mass.). As shown in FIG. 11, the levels of expression of endogenous PTP1B were decreased only in C57B16 cells transfected with the murine PTP1B sequence specific siRNAs.

[0230] The effect of RNAi on endogenous expression of murine PTP1B in a second murine cell line was examined. Mouse PTP1B:3T31R fibroblasts were transfected with 20 nM mPTP1B1.1 (SEQ ID NO:______); mPTP1B1.6 (SEQ ID NO:______); and mPTP1B1.8 (SEQ ID NO:______) according to the method described above. The level of murine PTP1B expression in the cells transfected with mPTPB11.1 decreased approximately 80% compared with cells transfected with a non-specific siRNA (hPTP1B1.3 (SEQ ID NO:______)); cells transfected with mPTP1B1.6 decreased approximately 40%; and cells transfected with mPTP1B1.8 decreased approximately 60%.

[0231] Interference with Murine PTP1B Expression by siRNA in Co-Transfection Assays

[0232] A recombinant expression construct was prepared that encodes wild-type murine PTP1B (mPTP1B) (GenBank Accession No. NM_(—)011201, SEQ ID NOs:______ and ______). The following oligonucleotide primers were used for the wild-type construct. The sequences of the BamHI and EcoRI restriction sites are underlined. mPTP1B-sense (mPTP1B 5′BamHI) (SEQ ID NO:   ) 5′-GGGGGGGATCCATGGAGATGGAGAAGGAGTTCGAGG-3′ mPTP1B anti sense (mPTP1B 3′EcoRI) (SEQ ID NO:   ) 5′-GGGGGAATTCTCAGTGAAAACACACCCGGTAGCAC-3′

[0233] Vector pCMVTag2B (Stratagene, La Jolla, Calif.) was digested with restriction endonuclease BamHI (New England Biolabs, Beverly, Mass.) for 3 hours at 37° C. The digested vector was then incubated with Klenow polymerase (New England Biolabs) for 15 minutes at 25° C. to fill in the recessed 3′ termini, followed by an incubation of 30 minutes at 37° C. with calf intestinal phosphatase (New England Biolabs). The GATEWAY™ Reading Frame Cassette B (Invitrogen Life Technologies, Carlsbad, Calif.) was inserted into the pCMVTag2B vector by ligation with T4 DNA ligase (Invitrogen Life Technologies) overnight at 16° C. according to the supplier's instructions. DB3.1™ competent E. Coli cells were transformed with the ligated vector (GWpCMVTag2) and DNA was isolated by standard molecular biology methods.

[0234] Vectors for expression of mPTP1 B wild type were prepared as follows. The mPTP1B construct was subcloned into a GATEWAY™ entry vector pENTR3 C™ (Invitrogen Life Technologies) by digesting 20 μl of the mPTP1B cDNA or 20 μl of the pENTR3C™ vector with 1 μl of BamHI (New England Biolabs); 1 μl of EcoRI (New England Biolabs); 5 μl 10×EcoRI buffer (New England Biolabs); 5 μl 10×BSA (New England Biolabs); and 18 μl distilled water for 3 hours at 37° C. Digested DNA was run on a 1% agarose gel, digested bands were excised, and the DNA was gel-purified using a QIAGEN Gel Extraction kit (QIAGEN, Inc., Valencia, Calif.). Four microliters of the mPTP1B cDNA was ligated into 2 μl of the pENTR3C™ vector overnight at 16° C. with 1 μl 10× Ligation Buffer (Invitrogen Life Technologies), 1 μl T4 DNA Ligase (4U/μl) (Invitrogen, Carlsbad, Calif.), and 2 μl distilled water. The construct was transformed into LIBRARY EFFICIENCY® DH5α™ cells. The FLAG® epitope-tagged mPTP1B construct was prepared by cloning the pENTR3 C™ mPTP1B WT construct into the GWpCMVTag2 vector. The pENTR3C™ construct containing the mPTP1B polynucleotide was linearized by digesting the construct with Vsp I (Promega Corp., Madison, Wis.) at 37° C. for 2 hours. The DNA was purified using a QIAGEN PCR Purification kit (QIAGEN, Inc.). Three microliters (100 ng/μl) of the GWpCMVTag2 vector were combined in a GATEWAY™ LR reaction with 6 μl linearized pENTR3C™ mPTP1B WT, 3 μl TE buffer, 4 μl Clonase™ Enzyme, and 4 μl LR reaction buffer (Invitrogen Life Technologies) for 1 hour at room temperature. After addition of Proteinase K (Invitrogen Life Technologies) to the reaction for 10 minutes, LIBRARY EFFICIENCY® DH5α™ cells were transformed with the expression construct.

[0235] The murine PTP1B expression vector (0.5 μg) was co-transfected with 20 nM murine PTP1B sequence-specific siRNA polynucleotides into PTP1B knockout mouse fibroblasts (PTP1B KO mouse embryonic fibroblasts were prepared from 13-day embryos from PTP1B knock out mice to establish the cell line, which was then transfected with human insulin receptor (1BKO+HIR) (HIR, Julie Moyers, Eli Lilly and Company, Indianapolis, Ind.)). Transfections were performed as described in Example 1. After incubating the transfected cells for 18 hours at 37° C., cell lysates were prepared, separated by 4-12% SDS-PAGE, and immunoblotted using the anti-PTP1B murine monoclonal antibody (see above). The results are summarized in Table 13. TABLE 12 siRNA INTERFERENCE WITH MURINE PTP-1B EXPRESSION IN CO-TRANSFECTION ASSAYS Related Decrease siRNA Sequence SEQ ID in Target (SEQ ID NO) siRNA Name NO: Expression Murine PTP1B 5′-gaagcccagaggagcuauatt-3′ mPTP1B1.1 95% 5′-cuacaccacauggccugactt-3′ mPTP1B1.2 Not analyzed 5′-gacugccgaccagcugcgctt-3′ mPTP1B1.3 Not analyzed 5′-gguaccgagaugucagccctt-3′ mPTP1B1.4 25% 5′-ugacuauaucaaugccagctt-3′ mPTP1B1.5 Not analyzed 5′-agaagaaaaggagaugguctt-3′ mPTP1B1.6 80% 5′-cgggaagugcaaggagcuctt-3′ mPTP1B1.7 Not analyzed 5′-ggaucaguggaaggagcuctc-3′ mPTP1B1.8 80%

[0236] Interference with Rat PTP1B Expression by siRNA in Co-Transfection Assays

[0237] A co-transfection assay was performed as described above in which 1BKO+HIR mouse fibroblasts were co-transfected with an expression vector containing the sequence encoding the peptide FLAG® in frame with a nucleotide sequence (SEQ ID NO:______) that encoded a rat PTP1B polypeptide (SEQ ID NO:______) (GenBank Accession No. NM_(—)102637) and a sequence specific siRNA, rPTP1B1.1 (5′-agaagaaaaagagaugguctt-3′ (SEQ ID NO:______)) (20 nM). Additional rat PTP1B specific siRNA polynucleotides examined in the co-transfection assay included rPTP1B1.2 (5′-cggaugguggguggagguctt-3′ (SEQ ID NO:______)); rPTP1B1.3 (5′-uggcaagugcaaggagcuctt-3′ (SEQ ID NO:______)); and rPTP1B1.4 (5′-cuacaccaccuggccugactt-3′ (SEQ ID NO:______)). The level of expression of the rat PTP1B polypeptide was determined by immunoblotting cell lysates with an anti-human PTP1B antibody that also specifically binds to rat PTP1B ((PHO2, Oncogene Research Products™, Inc. San Diego, Calif.). Expression of rat PTP1B decreased approximately 50% in cells transfected with rPTP1B1.1.

[0238] Interference with Human PTP-1B Expression by siRNA in Co-Transfection Assays

[0239] Human PTP1B encoding sequence was cloned into a Pmt vector according to standard molecular biology procedures (see Flint et al., EMBO J. 12:1937-46 (1993)). 1BKO+HIR cells were co-transfected with the human PTP-1B expression vector and siRNA polynucleotides (20 nM) specific for human PTP-1B sequences overnight using Lipofectamine 2000. Cells were lysed as described above, and the lysates were separated by 4-12% SDS-PAGE and transferred onto a PDVF membrane. The level of expression of human PTP-1B was determined by immunoblotting with an anti-human PTP-1B antibody (PHO2, Oncogene Research Products™, Inc. San Diego, Calif.). Interference with expression of human PTP-1B was observed with four siRNA polynucleotides as indicated in Table 14. TABLE 13 siRNA INTERFERENCE WITH HUMAN PTP-1B EXPRESSION IN CO-TRANSFECTION ASSAYS Related siRNA Sequence siRNA SEQ Decrease in Target (SEQ ID NO) Name ID NO: Expression Human PTP1B 5′-cuauaccacauggccugactt-3′ hPTP1B1.1 Not analyzed 5′-gcccaaaggaguuacauuctt-3′ hPTP1B1.2 >95% 5′-ggaagaaaaaggaagcccctt-3′ hPTP1B1.3 >95% 5′-caaugggaaaugcagggagtt-3′ hPTP1B1.4 >95% 5′-ggaucaguggaaggagcuutc-3′ hPTP1B1.5 >95%

[0240] Interference of Endogenous Expression of Human PTP-1B by siRNA

[0241] The effect of sequence specific siRNA on endogenous expression of human PTP-1B was examined in two different cell lines. HeLa cells were transfected as described above with HPTP1B1.1, hPTP1B1.2, hPTP1B1.3, hPTP1B1.4, and hPTP1B1.5 at 20 nM using Lipofectamine 2000, and after three days, the level of expression of PTP1B was analyzed by immunoblot. No significant decrease in expression of human PTP-1B was observed in HeLa cells transfected with the siRNA hPTP1B1.1. In HeLa cells transfected with hPTP1B1.2 and hPTP1B1.4, the level of expression of human PTP-1B decreased 80%, and in cells transfected with hPTP1B1.3, the level of expression decreased 90%. Endogenous expression of human PTP-1B in the second cell line, 293-HEK-HIR, (gift from Julie Moyers, Eli Lilly and Company) transfected with sequence specific siRNAs hPTP1B1.2, hPTP1B1.3, hPTP1B1.4, hPTP1B1.5 (20 nM) was reduced by 90%.

[0242] Interference with Expression of Murine TCPTP by siRNA in Co-Transfection Assays

[0243] A co-transfection assay was performed in which 1BKO+HIR murine fibroblasts were co-transfected as described above with an expression vector comprising a polynucleotide sequence (SEQ ID NO:______) encoding murine TCPTP (SEQ ID NO:______) and siRNA mTCPTP1.1 (5′-guugucaugcuaaaccgaact-3′ (SEQ ID NO:______)) (1 nM) or mTCPTP1.2 (5′-cagaacagagugaugguugag-3′ (SEQ ID NO:______)) (20 nM). The level of TCPTP expression was determined by immunoblotting with an anti-human TCPTP antibody (Curt Diltz, CEPTYR, Inc.). The siRNA mTCPTP1.2 did not interfere with expression of murine TCPTP. Expression of murine TCPTP decreased more than 95% in cells transfected with siRNA, mTCPTP1.1.

[0244] Interference with Expression of Human TCPTP by siRNA in Co-Transfection Assays

[0245] Co-transfection assays were performed essentially as described above for PTP1B expression analysis to determine siRNA inhibition of human TCPTP expression. A recombinant expression construct was prepared that encodes wild-type human TC45. The following oligonucleotide primers were used for the wild-type construct. The sequences of the BamHI and EcoRi restriction sites are underlined. Human TC45 sense (TC45 5′BamHI) 5′-GGGGGGATCCATGCCCACCACCATCGAGCGGGAGTT-3′ (SEQ ID NO   ) Human TC45 antisense (TC45 3′EcoRI) 5′-GGGGAATTCTTAGGTGTCTGTCAATCTTGGCCTTTTTCTTTTTCGTTCA-3′ (SEQ ID NO:   )

[0246] Vector pCMVTag2B (Stratagene, La Jolla, Calif.) was digested with restriction endonuclease BamHI (New England Biolabs, Beverly, Mass.) for 3 hours at 37° C. The digested vector was then incubated with Klenow polymerase (New England Biolabs) for 15 minutes at 25° C. to fill in the recessed 3′ termini, followed by an incubation of 30 minutes at 37° C. with calf intestinal phosphatase (New England Biolabs). The GATEWAY™ Reading Frame Cassette B (Invitrogen Life Technologies) was inserted into the pCMVTag2B vector by ligation with T4 DNA ligase (Invitrogen Life Technologies) overnight at 16° C. according to the supplier's instructions. DB3.1™ competent E. coli cells were transformed with the ligated vector (GWpCMVTag2) and DNA was isolated by standard molecular biology methods.

[0247] Vectors for expression of TC45 wild type were prepared as follows: The TC45 construct was subcloned into a GATEWAY™ entry vector pENTR3C™ (Invitrogen Life Technologies) by digesting 10 μl of the TC45 cDNA with 1 μl of BamHI (New England Biolabs), 1 μl of EcoRI (New England Biolabs), 3 μl 10×EcoRI buffer (New England Biolabs), 3 μl 10×BSA (New England Biolabs), and 12 μl distilled water for 3 hours at 37° C. Two microliters of the pENTR3C™ vector was digested with 0.5 μl of BamHI (New England Biolabs), 0.5 μl of EcoRI (New England Biolabs), 2 μl 10×EcoRI buffer (New England Biolabs), 2 μl 10×BSA (New England Biolabs), and 13 μl distilled water for 3 hours at 37° C., followed by an incubation of 30 minutes at 37° C. with calf intestinal phosphatase (New England Biolabs). Digested DNA was run on a 1% agarose gel, digested bands were excised and gel purified using a QIAGEN Gel Extraction kit (QIAGEN, Inc.). Four microliters of the TC45 cDNA was ligated into 2 μl of the pENTR3C™ vector overnight at 16° C. with 11 μl 10× Ligation Buffer (Invitrogen Life Technologies), 1 μl T4 DNA Ligase (4U/μl) (Invitrogen Life Technologies), and 2 μl distilled water. The construct was transformed into LIBRARY EFFICIENCY® DH5α™ cells. The FLAG® epitope-tagged TC45 construct was prepared by cloning the pENTR3C™ TC45 WT construct into the GWpCMVTag2 vector. The pENTR3C™ construct containing the TC45 polynucleotide was linearized by digesting the construct with Pvu I (New England Biolabs)) at 37° C. for 2 hours. The DNA was purified using a QIAGEN PCR Purification kit (QIAGEN, Inc.). Two microliters (150 ng/μl) of the GWpCMVTag2 vector were combined in a GATEWAY™ LR reaction with 3 μl linearized pENTR3C™ TC45 WT, 5 μl TE buffer, 4 μl Clonase™ Enzyme, and 4 μl LR reaction buffer (Invitrogen Life Technologies) overnight at room temperature. After addition of Proteinase K (Invitrogen Life Technologies) to the reaction for 10 minutes, LIBRARY EFFICIENCY® DH5α™ cells were transformed with the expression construct.

[0248] Cells (1BKO+HIR murine embryo fibroblasts) were co-transfected with an expression vector containing a nucleotide sequence encoding human TCPTP (SEQ ID NO:______) and siRNAs, hTCPTP1.4 (5′-guugucaugcugaaccgcatt-3′ (SEQ ID NO:______)) (20 nM); hTCPTP1.5 (5′-gcccauaugaucacagucgtg-3′ (SEQ ID NO:______)) (10 nM); hTCPTP1.6 (5′-ucgguuaaaugugcacaguac-3′ (SEQ ID NO:______)) (10 nM); or hTCPTP1.7 (5′-ugacuauccucauagaguggg-3′ (SEQ ID NO:______)) (20 nM). Additional human TCPTP specific siRNA polynucleotides were prepared; the sequences of each are as follows: hTCPTP1.1 (5′-agugagagaaucuggcucctt-3′ (SEQ ID NO:______)); hTCPTP1.2 (5′-ggaagacuuaucuccugcctt-3′ (SEQ ID NO:______)); and hTCPTP1.3 (5′-ggugaccgauguacaggactt-3′ (SEQ ID NO:______)). The level of TCPTP expression was determined by immunoblotting with an anti-human TCPTP antibody. The level of expression of human TCPTP was not affected by siRNA hTCPTP1.7. Expression levels decreased more than 95% in the cells co-transfected with hTCPTP1.4; 80% in cells co-transfected with hTCPTP1.5; and greater than 90% in cells transfected with hTCPTP1.6.

[0249] Interference of Endogenous Expression of Human TCPTP by siRNA

[0250] 293-HEK HIR cells were transfected with either hTCPTP1.4 (SEQ ID NO:______) or rPTP1B1.2, a rat PTP1B sequence specific siRNA (5′-cggaugguggguggagguctt-3′ (SEQ ID NO:______), which was included as a nonspecific siRNA control, at concentrations of 2, 5, 10, 20 and 50 nM. Endogenous expression of human TCPTP in the cells transfected with sequence specific hTCPTP1.4 decreased 90%.

[0251] Transient Transfection of Human PTP1B and Sequence Specific Hairpin Vectors

[0252] Effectiveness of a human PTP1B sequence-specific siRNA in the form of a hairpin insert was examined in a transient co-transfection assay. Cells (1BKO+HIR mouse fibroblasts) were transfected with a human PTP1B expression vector (see above) and co-transfected with hPTP1B hairpin vectors (1, 0.5, and 0.25 μg) according to the transfection method described above. The human PTP1B specific sequences were inserted in frame with a human U6 small nuclear RNA promoter into a vector, which was a gift from David Engelke (University of Michigan, Ann Arbor, Mich.) (see also Paul et al., Nat. Biotechnol. 20:446-48 (2002)). The sequences of each strand inserted into the hairpin vectors are as follows. hPTP1B H1.2-HP4 5′-tttGCCCAAAGGAGTTACATTCGTAAGAATGTAACTCCTTTGGGCttttt-3′ (SEQ ID NO:   ) 3′ GGGTTTCCTCAATGTAAGCATTCTTACATTGAGGAAACCCGaaaaagatc-5′ (SEQ ID NO:   ) hPTP1B H1.2-HP9 5′-tttGCCCAAAGGAGTTACATTCCCTGGGTAAGAATGTAACTCCTTTGGGCttttt-3′ (SEQ ID NO:   ) 3′ GGGTTTCCTCAATGTAAGGGACCCATTCTTACATTGAGGAAACCCGaaaaagatc-5′ (SEQ ID NO:   )

[0253] Twenty-four hours after the cells were transfected, cell lysates were prepared and expression of human PTP1B was determined by immunoblotting with an antihuman PTP1B antibody (see above). Cell lysates were also immunoblotted with an antibody specific for human insulin receptor beta chain (IRβ) (Cat. No. C-19, Santa Cruz Biotechnology). The results are presented in FIG. 19.

[0254] Hairpin vectors are also prepared that contain sequences specific for murine PTP1B. The following sequences of each strand are inserted into a hairpin vector. mPTP1BM1.1-HP4 5′-tttGAAGCCCAGAGGAGCTATAAGAATATAGCTCCTCTGGGCTTCttttt-3′ (SEQ ID NO:   ) 3′ TTCGGGTCTCCTCGATATTCTTATATCGAGGAGACCCGAAGaaaaagatc-5′ (SEQ ID NO:   ) mPTP1BM1.1-HP9 5′-tttGAAGCCCAGAGGAGCTATAGGGTGAGAATATAGCTCCTCTGGGCTTCttttt-3′ (SEQ ID NO:   ) 3′ TTCGGGTCTCCTCGATATCCCACTCTTATATCGAGGAGACCCGAAGaaaaagatc-5′ (SEQ ID NO:   )

EXAMPLE 6 Regulatory Role of TCPTP in Insulin Signaling

[0255] The protein tyrosine phosphatase TC-PTP exists in two alternatively spliced forms, TC45 and TC48, that share the same catalytic domain but differ at their extreme carboxy-termini (Mosinger et al., Proc. Natl. Acad. Sci. USA 89:499-503 (1992)). Insulin-induced oxidation and inactivation of TC45 suggested that it functions as a negative regulator of insulin signaling (see U.S. Ser. No. 10/366,547). This Example examines the regulatory role of TC45 in insulin signaling by inhibiting expression of the PTP by RNAi.

[0256] The specific siRNA duplexes were designed by first scanning through the open reading frame of TC45 mRNA and selecting sequences of 5′AA(N₁₉)3′ (N=any nucleotide) for further characterization. The following 2 oligonucleotides were chosen: 5′-AACAGAUACAGAGAUGUAAGC-3′ (TCPTP1) (SEQ ID NO:______) and 5′-AAGCCCA UAUGAUC ACAGUCG-3′ (TCPTP2) (SEQ ID NO:______). These sequences were submitted to a BLAST search against human, rat, and mouse genome databases to ensure specificity for TC-PTP. The 21-nt siRNA duplexes were obtained in a deprotected and desalted form (Dharmacon Research). Rat-1 fibroblasts (Fischer rat fibroblast 3T3 like cell line) and HepG2 (human hepatocellular carcinoma) cells (American Type Culture Collection (ATCC), Manasass, Va.) were transfected with each siRNA at 100 nM. Both siRNA oligonucleotides suppressed expression of endogenous TC45 in the transfected HepG2 cells and Rat-1 fibroblasts, with TCPTP1 being more efficient.

[0257] Rat-1 (fibroblasts) and HepG2 (human hepatocellular carcinoma) cells were routinely maintained in DMEM supplemented with 10% FBS, 1% glutamine, 100 U/ml penicillin and 100 μg/ml streptomycin. For stimulation with insulin, cells were plated in media containing 10% FBS for 48 hours, then serum-starved for 16 hours before treatment. For transient transfection, cells were plated in DMEM supplemented with 10% FBS for 16 hours, then in OptiMEM (Invitrogen) without serum, after which the plasmid (5 μg/dish for Rat-1,30 μg/dish for HepG2) was introduced by LipofectAMINE and PLUS reagents (Invitrogen), according to the manufacture's recommendations. The transfection efficiency was routinely 40%. For RNAi experiments, cells were plated as above and the TCPTP siRNA duplexes were introduced by Oligofectamine (Invitrogen) according to the guidelines provided by Dharmacon Research Inc.

[0258] The potential regulatory role of TC45 in insulin signaling was investigated by examining the phosphorylation status of PKB/Akt, which is a critical effector in the P13 kinase pathway that mediates various intracellular responses to insulin, following ablation of the PTP by RNAi. The human hepatoma cell line HepG2 has been used extensively as a model to study insulin signaling (see Huang et al., J. Biol. Chem. 277:18151-60 (2002); Haj et al., Science 295 1708-11 (2002)). Serum-deprived Rat-I and HepG2 cells were exposed to 10 or 50 nM insulin for 5 min and lysed. The insulin receptor (IR) was immunoprecipitated from 500 μg of cell lysate with anti-IR-β antibody 29B4 (Santa Cruz Biotechnology), then immunoblotted with anti-phosphotyrosine, anti-pYpY^(1162/1162)-IR-β (Biosource International, Camarillo, Calif.) and anti-IR-β (C-19) (Santa Cruz Biotechnology) antibodies. HepG2 cells expressed higher levels of IR-β than Rat-1 cells as shown in FIG. 20A and displayed a robust response to insulin stimulation, as shown by the overall tyrosine phosphorylation level of IR-β and autophosphorylation of the activation loop tyrosines 1162 and 1163 (see FIG. 20A).

[0259] For the RNAi experiment, HepG2 cells were untransfected (control) or transfected (+siRNA) with 100 nM siRNA TCPTP1 oligonucleotide. Two days after transfection, cells were serum-starved for 16 hours and then stimulated with 10 nM insulin for 0, 1, 2, 5, 10, and 20 minutes. Total lysates (30 μg) were immunoblotted with anti-phospho-PKB/Akt (Cell Signaling Technology, Beverly, Mass.); anti-PKB/Akt (Cell Signaling Technology); anti-TC45 (1910H (Lorenzen et al., J. Cell. Biol. 131:631-43 (1995))); and anti-PTP1B (FG6 (LaMontagne et al., Mol. Cell. Biol. 18:2965-75 (1998))) antibodies. The results presented in FIG. 20B indicate that depletion of TC45 enhanced both the intensity and duration of the signaling response. FIG. 20C illustrates a densitometric analysis of the gel image to show the ratio of phosphorylated PKB/Akt relative to total PKB/Akt. Similar results were observed in three independent experiments.

[0260] The role of TC45 in insulin signaling was further investigated by preparing a TC45 substrate trapping mutant. Substitution of an alanine residue for the invariant aspartate, which functions as a general acid in catalysis, into the vector expressing TC45 and into a vector expressing PTP1B was performed by standard site-directed mutagenesis protocols. HepG2 cells overexpressing wild type (WT) or trapping mutant (DA) forms of PTP1B and TC45 were either left untreated (−INS) or stimulated with 10 nM insulin for 5 min (+INS), then lysed in trapping buffer (20 mM Tris (pH 7.4), 1% NP-40, 150 mM NaCl, 10% glycerol, 10 mM IAA and 25 μg/ml each of aprotinin and leupeptin). Aliquots (1 mg) of cell lysate were incubated with anti-PTP1B antibody (FG6) or anti-TC45 antibody (CF4). The immunocomplexes were washed with lysis buffer, subjected to SDS-PAGE then immunoblotted with anti-IR-β (C-19) antibody. An aliquot of lysate (30 μg) was immunoblotted with anti-PTP1B antibody (FG6) or anti-TC-PTP antibody (CF4) to verify PTP expression. The data are shown in FIG. 21A and are representative of three independent experiments. These data suggest that TC45 recognizes IR-β as a substrate.

[0261] Serum starved, untransfected (control) or TC45 siRNA (100 nM) transfected (+siRNA) HepG2 cells were stimulated with 10 nM insulin for 0, 1, 2, 5, 10, and 20 minutes. The insulin receptor was immunoprecipitated from 750 μg of cell lysate with anti-IR-β antibody 29B4 and immunoblotted with anti-phosphotyrosine (G104), anti-pY⁹⁷²-β (Biosource), anti-pYpY^(1162/1163)-IR-β, and anti-IR-β (C-19) antibodies as shown in FIG. 21B. FIG. 21C illustrates densitometric analyses of the gel image to show the ratio of phosphorylated IR-β relative to total IR-β for total phosphotyrosine (upper panel), phosphorylation of Tyr 972 (middle panel), and phosphorylation of the activation loop tyrosines 1162 and 1163 (lower panel). Similar results were observed in two independent experiments.

EXAMPLE 7 Effect of siRNAs Specific for PTP1B and TCPTP on Insulin Receptor Tyrosine Phosphorylation

[0262] This example illustrates the effect of RNAi on the function of components in a cell signaling pathway. The role of PTP1B in the down regulation of insulin signaling has been illustrated by data derived from a variety of approaches (Cheng et al., Eur. J. Biochem. 269:1050-59 (2002)), including the phenotype of the PTP1B knockout mouse (Elchebly et al., Science 283:1544-48 (1999); Klaman et al., Mol. Cell Biol 20:5479-89 (2000); see also U.S. patent application Ser. No. 10/366,547).

[0263] The effect of human PTP1B siRNA and of human TCPTP siRNA on the level of phosphorylation of IR-β was evaluated by ELISA. 292-HEK HIR cells were transfected with 0, 0.5, 3, or 10 nM siRNAs. The siRNA polynucleotides transfected into the cells included hPTP1B1.2 (SEQ ID NO:______), hPTP1B1.3 (SEQ ID NO:______), mPTP1B1.1 (SEQ ID NO:______), rPTP1B1.2 (SEQ ID NO:______), hTCPTP1.4 (SEQ ID NO:______), and the combination of hPTP1B1.3 and hTCPTP1.4. Seventy-two hours after transfection, cells were exposed to insulin for 7 minutes at concentrations of 0, 25, 50, 75, and 100 nM. Cell lysates were prepared as described in Example 1, and total cell protein was quantified by the Bio-Rad Protein Assay performed according to the manufacturer's instructions (BioRad, Hercules, Calif.). An ELISA was performed as follows. Dynex Immulon HB4X plates were coated with anti-insulin receptor antibody Ab-1 (1 mg/ml; NeoMarkers, Inc., Fremont, Calif.) that was diluted 1:1000 in CMF (calcium magnesium free)-PBS containing 5 μg/ml fatty acid free BSA (faf-BSA). The plates were incubated at 4° C. for at least four hours. The antibody solution was removed by aspiration, followed by the addition of 300 μl of 3% faf-BSA+CMF-PBS. The plates were incubated for 1 hr with agitation on a vortex platform shaker (setting #5) at room temperature. After aspirating the 3% faf-BSA+CMF-PBS solution, approximately 10-20 μg of lysate were added to the wells and incubated at room temperature for one hour. Plates were washed three times with TBST (20 mM Tris-HCl, pH 7.5 150 mM NaCl; 0.05% Tween 20). An anti-insulin receptor phosphotyrosine specific antibody (pTyr 1162/63, Biosource International, Camarillo, Calif., Catalog #44-804) was diluted 1:2000 in TBST and added to the plates for one hour at room temperature. The plates were washed three times with TBST. HRP-conjugated anti-rabbit antibody (Amersham Biosciences, catalog #NA934V) (1:2000 in TBST) was then added to the wells and incubated at room temperature for one hour. The plates were washed three times with TBST and once with deionized, sterile water. TMB solution (Sigma Aldrich) (100 μl per well) was added and developed until a modest color change (10-30 minutes depending on cell type and insulin response). The reaction was stopped with 100 μl of 1.8 N H₂SO₄ and then mixed. The optical density of each well was measured at 450 nM in a Spectramax plate reader (Molecular Devices Corp., Sunnyvale, Calif.). The data are presented in FIG. 22. The level of expression of PTP1B in each cell lysates was determined by immunoblot as described above. PTP1B polypeptide was detected using an anti-human PTP-1B antibody (PHO2, Oncogene Research Products™, Inc.). The amount of PTP1B expressed in cells transfected with varying concentrations of either siRNA was quantified by densitometric analysis of the immunoblot. The level of expression of human PTP1B is presented as a percent of the level of expression in cells that were not transfected with hPTP1B1.3 siRNA (i.e., the level of expression in untransfected cells equals 100%) (see tables in FIG. 22).

[0264] In a second experiment, 292-HEK HIR cells were transfected with 0, 0.5, 3, or 10 nM siRNAs. The siRNA polynucleotides transfected into the cells included hPTP1B1.2 (SEQ ID NO:______), hPTP1B1.3 (SEQ ID NO:______), mPTP1B1.1 (SEQ ID NO:______), hTCPTP1.4 (SEQ ID NO:______), and rPTP1B1.2 (SEQ ID NO:______). Seventy-two hours after transfection, cells were exposed to insulin for 7 minutes at concentrations of 0, 5, 10, 20, 50, and 100 nM. Cell lysates were prepared and total cell protein was quantified as described above. An ELISA was performed as described above. Cell lysates were coated onto 96-well plates, blocked, and probed with an anti-pYpY^(1162/1163)-IR-β antibody. Binding was detected using an enzyme conjugated secondary reagent. As shown in FIGS. 23 and 24, respectively, increased phosphorylation of the insulin receptor was observed in cells transfected with hPTP1B1.3 and with hTCPTP1.4.

[0265] The percent decrease in the level of PTP1B expression was compared with the level of phosphorylation of the insulin receptor. In three separate experements, 292-HEK HIR cells were transfected with 0, 0.5, 3, or 10 nM hPTP1B1.3 siRNA and then exposed to insulin for 7 minutes at concentrations of 0, 5, 10, 20, 50, and 100 nM. An ELISA and immunoblot of cell lysates were performed as described above. The effect of hPTP1B1.3 siRNA on the phosphorylation state of the insulin receptor is summarized in FIG. 25. Each data point represents the average optical density measured in duplicate wells.

EXAMPLE 8 Identification of Oncology Targets and Decreased Expression of the Targets by Specific siRNAs

[0266] This Example describes validation of DSP-3 as a target for oncology therapeutics. The Example also describes identification of siRNA polynucleotides that effectively interfere with expression of known chemotherapeutic target polypeptides.

[0267] Expression of DSP-3 polypeptide was evaluated in several cancer cell lines transfected with sequence specific DSP-3 siRNA polynucleotides and nonspecific siRNA polynucleotides. Cell lines included HeLa, HS578T; MDA-MB-231; MDA-MB-435 (breast cancer cell line that is ER⁻, Her²⁺, EGFR⁺, p53^(mut), and invasive); MCF7 (breast cancer cell line that is ER⁺, Her2^(low), EGFR^(low), p53^(WT), and non-invasive); T47D (breast cancer cell line that is ER⁺, Her2⁻, EGFR⁻, p53^(mut), and non-invasive); HCT-116 (p53^(WT)); and HT-29 (p53^(mut)). Cells were transfected with 10 nM DSP3.1 (SEQ ID NO:______), DSP3.4 (5′-ggugacacauauucugucutt-3′, (SEQ ID NO:______)), or Scr.2 (SEQ ID NO:______) (scrambled, a non-specific siRNA sequence not found in a human genome database), and then cell lysates were prepared and evaluated for expression of DSP-3 and inhibition of expression by specific siRNAs, as described in Example 1. Transfection efficiency of some cell lines with siRNA, for example, MC7 and T47D, was improved by using Lipofectamine™ 2000 according to manufacturer's recommendations (Invitrogen Life Technologies) rather than Oligofectamine™ (Invitrogen Life Technologies) for the transfection procedure. The level of expression of DSP-3 polypeptide in the presence of specific siRNA 4compared with the non-specific siRNA control was significantly decreased in MCF7, T47D, MD-MB-435, HCT-116, and HT-29 cells.

[0268] Interference with expression of known chemotherapeutic targets by RNAi was examined, and siRNA polynucleotides that effectively interfere with expression of the targets were identified. Targets included dihydrofolate reductase (DHFR) (GenBank Accession No. NM_(—)000791) (SEQ ID NOs:______ and ______); thymidylate synthetase (GenBank Accession No. NM_(—)001071) (SEQ ID NOs:______ and ______); and topoisomerase I (GenBank Accession No. J03250) (SEQ ID NOs:______ and ______). The siRNA polynucleotides were designed according to methods described in Examples 1 and 2 and were manufactured by Dharmacon. Each siRNA was transfected into HeLa cells, and the effect of each on the endogenous expression of DHFR, thymidylate synthetase, and topoisomerase I was evaluated by immunoblotting of cell lysates as described in Example 1. The level of expression of the targets was determined by immunoblotting with an anti-DHFR monoclonal antibody (BD monoclonal antibody (diluted 1:250)); an anti-topoisomerase I antibody (Santa Cruz Biotechnology, Cat. No. sc-10783, diluted 1:200); and an anti-thymidylate synthetase antibody (Rockland sheep polyclonal antibody diluted 1:2000). The results are presented in Table 3. TABLE 14 siRNA INTERFERENCE WITH ENDOGENOUS EXPRESSION OF DHFR, THYMIDYLATE SYNTHETASE, AND TOPOISOMERASE I Related siRNA Sequence siRNA SEQ Decrease in Target (SEQ ID NO) Name ID NO: Expression DHFR 5′-gaccugguucuccauuccutt-3′ DHFR.1 >90% 5′-gcaguguauuugcuagguctt-3′ DHFR.3 >80% 5′-gucagcgagcagguucucatt-3′ DHFR.4 >90% Thymidylate 5′-ccaaacguguguucuggaatt-3′ TYMS.1 >95% Synthetase 5′-ccaacccugacgacagaagtt-3′ TYMS.2 >90% 5′-gccaggugacuuuauacactt-3′ TYMS.3 >95% 5′-cccagaccuuucccaaagctt-3′ TYMS.4 >90% Topoisomerase I 5′-gauagagccuccuggacuutt-3′ TOP1.1 >90% 5′-guccggcaugauaacaaggtt-3′ TOP1.2 >90% 5′-ggagaaacagcggacacugtt-3′ TOP1.3 >80% 5′-gcagcccgaggaugaucuutt-3′ TOP1.4 >80%

[0269] Interference of expression of another chemotherapeutic polypeptide target IKKgamma is performed according to the same procedures described above. The siRNA polynucleotides that are tested are IKK.1 (5′-gagucuccucuggggaagctt-3′ (SEQ ID NO:______)); IKK.2 (5′-ggaguuccucaugugcaagtt-3′ (SEQ ID NO:______)); IKK.3 (5′-ggccucugugaaagcccagtt-3′ (SEQ ID NO:______)); and IKK.4 (5′-cacgcugcucuugauguggtt-3′ (SEQ ID NO:______)).

[0270] The effect of RNAi silencing on expression of DHFR was compared with silencing of DSP-3, Cdc14a, and SHP-2 polypeptide expression in a HCT-116 cell proliferation assay. HCT-116 cells were transfected with 2.5 nM of the following siRNA oligonucleotides: scr.2 (SEQ ID NO:______); DSP3.1 (SEQ ID NO:______); DSP3.4 (SEQ ID NO:______); cdc14a.3 (SEQ ID NO:______); cdc14a.5 (SEQ ID NO:______); SHP2.1 (SEQ ID NO:______); SHP2.2 (SEQ ID NO:______); and DHFR.1 (SEQ ID NO:______). After 5 days, cell proliferation was evaluated by performing an MTT assay essentially as described in Example 4. The results are presented in FIG. 26. The optical density (OD) measured for each siRNA represents an average of six wells.

[0271] A cell proliferation assay was also performed using a different cell line, T47D, and the same siRNAs. The data are presented in FIG. 27. The effect of silencing on proliferation was confirmed by cell counting. The number of T47D cells transfected with the nonspecific control siRNA scr.2 was approximately 200×10⁴. In T47D cells transfected with either DSP3.1 or DSP3.4 siRNA, the number of cells was approximately 75% of the negative control, and in the presence of DHFR.1, the number of cells was approximately 50% compared with cells transfected with the nonspecific control. Significantly decreased expression of DSP-3 and DHFR in cells transfected with the respective siRNAs was confirmed by immunoblot.

[0272] Silencing of DSP-3 in HCT-116 and T47D cells also induced proapoptotic signaling. HCT-116 cells and T47D cells were transfected with 10 nM of non-specific si RNA control scrb1.2 (SEQ ID NO:______) (identical sequence to scr.2 described above), DSP3.1, DSP3.4, or DHFR.1. Three days after transfection of HCT-116 cells and five days after transfection of T47D cells, PARP assays were performed as described in Example 4. The results are presented in FIG. 28.

EXAMPLE 9 Inhibition of MAP Kinase Kinase Expression by RNAi

[0273] This Example describes interference of expression of MAP kinase kinases that are involved in the JNK signal transduction pathway in cells transfected with sequence specific siRNA polynucleotides.

[0274] Transient co-transfection experiments were performed as described in Example 2. 293-HEK cells were co-transfected with an expression vector that contained a polynucleotide sequence (GenBank Accession No. L36870 (SEQ ID NO:______)) that encoded FLAG®-tagged human MKK4 polypeptide (GenBank Accession No. L36870 (SEQ ID NO:______)) or with an expression vector that contained a polynucleotide sequence (GenBank Accession No. AF013588 (SEQ ID NO:______)) that encoded FLAG®-tagged human MKK7 polypeptide (GenBank Accession No. AF013588 (SEQ ID NO:______)). The siRNA oligonucleotides were designed and prepared as described in Examples 1 and 2. The cells were transfected and the level of expression of each kinase was determined by immunoblotting with an anti-FLAG® monoclonal antibody as described in Example 2. The results are presented in Table 4. TABLE 15 siRNA INTERFERENCE WITH MKK4 AND MKK7 EXPRESSION IN CO-TRANSFECTION ASSAYS siRNA Sequence Related Decrease in Target (SEQ ID NO) siRNA Name SEQ ID NOs Expression MKK4 5′-gugggcaaauaauggcagutt-3′ MKK4.1 80% 5′-cugugaaagcacuaaaccatt-3′ MKK4.2 90% 5′-ggagauccuccgcagcugatt-3′ MKK4.3 90% 5′-gcucuuuauacuuuggccutt-3′ MKK4.4 80% MKK7 5′-gcagacgggcuaccugacctt-3′ MKK7.1 10% 5′-cacggacgucuucaucgcctt-3′ MKK7.2 10% 5′-gaagcggaugcagggcccctt-3′ MKK7.3 10% 5′-cugcaagacggacuuugagtt-3′ MKK7.4 10%

EXAMPLE 10 Inhibition of Human P53 Expression by RNAi

[0275] An hairpin vector is prepared that contains a polynucleotide insert comprising a sequence that is a portion of a polynucleotide that encodes human p53 as described in Example 5. This sequence may be incorporated into a hairpin vector and transfected into a cell line known to express p53 (see Example 5). The level of expression of p53 is then determined by methods well known in the art, such as immunoblotting using an anti-p53 antibody (see Example 5). The p53 sequence incorporated into a hairpin vector is as follows.

[0276] HP53-HP9

[0277] 5′-tttGACTCCAGTGGTMTCTACTTCMGAGAGTAGATTACCACTGGAGTCttttt-3′ (SEQ ID NO:______)

[0278] 3′ tgaggtcaccattagatgaagttctctcatctaatggtgacctcagAAAAAGATC-5′ (SEQ ID NO:______)

ADDITIONAL REFERENCES

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[0282] Carthew, Richard W., Current Opinion in Cell Biology 13:244-248 (2001)

[0283] Clemens et al., Proc. Natl. Acad. Sci. USA 97:6499-6503 (2000)

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[0316] WO 01/96584

[0317] WO 99/32619

[0318] From the foregoing, it will be appreciated that, although specific embodiments of the invention have been described herein for the purpose of illustration, various modifications may be made without deviating from the spirit and scope of the invention. Accordingly, the present invention is not limited except as by the appended claims.

0 SEQUENCE LISTING <160> NUMBER OF SEQ ID NOS: 842 <210> SEQ ID NO 1 <211> LENGTH: 7 <212> TYPE: PRT <213> ORGANISM: Unknown <220> FEATURE: <223> OTHER INFORMATION: Unique signature sequence motif contained within the conserved domain of the PTP family of enzymes <220> FEATURE: <221> NAME/KEY: VARIANT <222> LOCATION: 2, 3, 4, 5, 6 <223> OTHER INFORMATION: Xaa = Any Amino Acid <400> SEQUENCE: 1 Cys Xaa Xaa Xaa Xaa Xaa Arg 1 5 <210> SEQ ID NO 2 <211> LENGTH: 11 <212> TYPE: PRT <213> ORGANISM: UNKNOWN <220> FEATURE: <223> OTHER INFORMATION: 11 amino acid conserved sequence conatining the signature sequence motif for the majority of PTPs. <220> FEATURE: <221> NAME/KEY: VARIANT <222> LOCATION: 1 <223> OTHER INFORMATION: Xaa = Ile or Val <220> FEATURE: <221> NAME/KEY: VARIANT <222> LOCATION: 4,7,8 <223> OTHER INFORMATION: Xaa = any amino acid <220> FEATURE: <221> NAME/KEY: VARIANT <222> LOCATION: 10 <223> OTHER INFORMATION: Xaa = Ser or Thr <400> SEQUENCE: 2 Xaa His Cys Xaa Ala Gly Xaa Xaa Arg Xaa Gly 1 5 10 <210> SEQ ID NO 3 <211> LENGTH: 21 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - DSP3.1 <400> SEQUENCE: 3 cgauagugcc aggccuaugt t 21 <210> SEQ ID NO 4 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - DSP3.1 <400> SEQUENCE: 4 cgauagugcc aggccuaug 19 <210> SEQ ID NO 5 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - DSP3.1 <400> SEQUENCE: 5 cauaggccug gcacuaucg 19 <210> SEQ ID NO 6 <211> LENGTH: 21 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - DSP3.1 <220> FEATURE: <221> NAME/KEY: misc_feature <222> LOCATION: 20, 21 <223> OTHER INFORMATION: n = A,T,C,G or U <400> SEQUENCE: 6 cgauagugcc aggccuaugn n 21 <210> SEQ ID NO 7 <211> LENGTH: 21 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - DSP3.1 <220> FEATURE: <221> NAME/KEY: misc_feature <222> LOCATION: 1, 2 <223> OTHER INFORMATION: n = A,T,C,G or U <400> SEQUENCE: 7 nncauaggcc uggcacuauc g 21 <210> SEQ ID NO 8 <211> LENGTH: 21 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - DSP3.2 <400> SEQUENCE: 8 gcaugagguc caucaguaut t 21 <210> SEQ ID NO 9 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - DSP3.2 <400> SEQUENCE: 9 gcaugagguc caucaguau 19 <210> SEQ ID NO 10 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - DSP3.2 <400> SEQUENCE: 10 auacugaugg accucaugc 19 <210> SEQ ID NO 11 <211> LENGTH: 21 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - DSP3.2 <220> FEATURE: <221> NAME/KEY: misc_feature <222> LOCATION: 20, 21 <223> OTHER INFORMATION: n = A,T,C,G or U <400> SEQUENCE: 11 gcaugagguc caucaguaun n 21 <210> SEQ ID NO 12 <211> LENGTH: 21 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - DSP3.2 <220> FEATURE: <221> NAME/KEY: misc_feature <222> LOCATION: 1, 2 <223> OTHER INFORMATION: n = A,T,C,G or U <400> SEQUENCE: 12 nnauacugau ggaccucaug c 21 <210> SEQ ID NO 13 <211> LENGTH: 21 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - DSP3.3 <400> SEQUENCE: 13 cgauacugcc aggcccaugt t 21 <210> SEQ ID NO 14 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - DSP3.3 <400> SEQUENCE: 14 cgauacugcc aggcccaug 19 <210> SEQ ID NO 15 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - DSP3.3 <400> SEQUENCE: 15 caugggccug gcaguaucg 19 <210> SEQ ID NO 16 <211> LENGTH: 21 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - DSP3.3 <220> FEATURE: <221> NAME/KEY: misc_feature <222> LOCATION: 20, 21 <223> OTHER INFORMATION: n = A,T,C,G or U <400> SEQUENCE: 16 cgauacugcc aggcccaugn n 21 <210> SEQ ID NO 17 <211> LENGTH: 21 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - DSP3.3 <220> FEATURE: <221> NAME/KEY: misc_feature <222> LOCATION: 1, 2 <223> OTHER INFORMATION: n = A,T,C,G or U <400> SEQUENCE: 17 nncaugggcc uggcaguauc g 21 <210> SEQ ID NO 18 <211> LENGTH: 21 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - MKP.1 <400> SEQUENCE: 18 auccugcccu uucuguacct t 21 <210> SEQ ID NO 19 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - MKP.1 <400> SEQUENCE: 19 auccugcccu uucuguacc 19 <210> SEQ ID NO 20 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - MKP.1 <400> SEQUENCE: 20 gguacagaaa gggcaggau 19 <210> SEQ ID NO 21 <211> LENGTH: 21 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - MKP.1 <220> FEATURE: <221> NAME/KEY: misc_feature <222> LOCATION: 20, 21 <223> OTHER INFORMATION: n = A,T,C,G or U <400> SEQUENCE: 21 auccugcccu uucuguaccn n 21 <210> SEQ ID NO 22 <211> LENGTH: 21 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - MKP.1 <220> FEATURE: <221> NAME/KEY: misc_feature <222> LOCATION: 1, 2 <223> OTHER INFORMATION: n = A,T,C,G or U <400> SEQUENCE: 22 nngguacaga aagggcagga u 21 <210> SEQ ID NO 23 <211> LENGTH: 21 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - MKP.2 <400> SEQUENCE: 23 gcagaggcaa agcaucauct t 21 <210> SEQ ID NO 24 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - MKP.2 <400> SEQUENCE: 24 gcagaggcaa agcaucauc 19 <210> SEQ ID NO 25 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - MKP.2 <400> SEQUENCE: 25 gaugaugcuu ugccucugc 19 <210> SEQ ID NO 26 <211> LENGTH: 21 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - MKP.2 <220> FEATURE: <221> NAME/KEY: misc_feature <222> LOCATION: 20, 21 <223> OTHER INFORMATION: n = A,T,C,G or U <400> SEQUENCE: 26 gcagaggcaa agcaucaucn n 21 <210> SEQ ID NO 27 <211> LENGTH: 21 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - MKP.2 <220> FEATURE: <221> NAME/KEY: misc_feature <222> LOCATION: 1, 2 <223> OTHER INFORMATION: n = A,T,C,G or U <400> SEQUENCE: 27 nngaugaugc uuugccucug c 21 <210> SEQ ID NO 28 <211> LENGTH: 21 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - cdc14a.1 <400> SEQUENCE: 28 caucgugcga agguuccugt t 21 <210> SEQ ID NO 29 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - cdc14a.1 <400> SEQUENCE: 29 caucgugcga agguuccug 19 <210> SEQ ID NO 30 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - cdc14a.1 <400> SEQUENCE: 30 caggaaccuu cgcacgaug 19 <210> SEQ ID NO 31 <211> LENGTH: 21 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - cdc14a.1 <220> FEATURE: <221> NAME/KEY: misc_feature <222> LOCATION: 20, 21 <223> OTHER INFORMATION: n = A,T,C,G or U <400> SEQUENCE: 31 caucgugcga agguuccugn n 21 <210> SEQ ID NO 32 <211> LENGTH: 21 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - cdc14a.1 <220> FEATURE: <221> NAME/KEY: misc_feature <222> LOCATION: 1, 2 <223> OTHER INFORMATION: n = A,T,C,G or U <400> SEQUENCE: 32 nncaggaacc uucgcacgau g 21 <210> SEQ ID NO 33 <211> LENGTH: 21 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - CD45.2 <400> SEQUENCE: 33 gccgagaaca aaguggaugt t 21 <210> SEQ ID NO 34 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - CD45.2 <400> SEQUENCE: 34 gccgagaaca aaguggaug 19 <210> SEQ ID NO 35 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - CD45.2 <400> SEQUENCE: 35 cauccacuuu guucucggc 19 <210> SEQ ID NO 36 <211> LENGTH: 21 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - CD45.2 <220> FEATURE: <221> NAME/KEY: misc_feature <222> LOCATION: 20, 21 <223> OTHER INFORMATION: n = A,T,C,G or U <400> SEQUENCE: 36 gccgagaaca aaguggaugn n 21 <210> SEQ ID NO 37 <211> LENGTH: 21 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - CD45.2 <220> FEATURE: <221> NAME/KEY: misc_feature <222> LOCATION: 1, 2 <223> OTHER INFORMATION: n = A,T,C,G or U <400> SEQUENCE: 37 nncauccacu uuguucucgg c 21 <210> SEQ ID NO 38 <211> LENGTH: 8 <212> TYPE: PRT <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: FLAG sequence <400> SEQUENCE: 38 Asp Tyr Lys Asp Asp Asp Asp Lys 1 5 <210> SEQ ID NO 39 <211> LENGTH: 21 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - DSP11.2 <400> SEQUENCE: 39 cuggcaccau gcuggccugt t 21 <210> SEQ ID NO 40 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - DSP11.2 <400> SEQUENCE: 40 cuggcaccau gcuggccug 19 <210> SEQ ID NO 41 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - DSP11.2 <400> SEQUENCE: 41 caggccagca uggugccag 19 <210> SEQ ID NO 42 <211> LENGTH: 21 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - DSP11.2 <220> FEATURE: <221> NAME/KEY: misc_feature <222> LOCATION: 20, 21 <223> OTHER INFORMATION: n = A,T,C,G or U <400> SEQUENCE: 42 cuggcaccau gcuggccugn n 21 <210> SEQ ID NO 43 <211> LENGTH: 21 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - DSP11.2 <220> FEATURE: <221> NAME/KEY: misc_feature <222> LOCATION: 1, 2 <223> OTHER INFORMATION: n = A,T,C,G or U <400> SEQUENCE: 43 nncaggccag cauggugcca g 21 <210> SEQ ID NO 44 <211> LENGTH: 21 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - DSP11.4 <400> SEQUENCE: 44 agcagucuuc caguucuact t 21 <210> SEQ ID NO 45 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - DSP11.4 <400> SEQUENCE: 45 agcagucuuc caguucuac 19 <210> SEQ ID NO 46 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - DSP11.4 <400> SEQUENCE: 46 guagaacugg aagacugcu 19 <210> SEQ ID NO 47 <211> LENGTH: 21 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - DSP11.4 <220> FEATURE: <221> NAME/KEY: misc_feature <222> LOCATION: 20, 21 <223> OTHER INFORMATION: n = A,T,C,G or U <400> SEQUENCE: 47 agcagucuuc caguucuacn n 21 <210> SEQ ID NO 48 <211> LENGTH: 21 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - DSP11.4 <220> FEATURE: <221> NAME/KEY: misc_feature <222> LOCATION: 1, 2 <223> OTHER INFORMATION: n = A,T,C,G or U <400> SEQUENCE: 48 nnguagaacu ggaagacugc u 21 <210> SEQ ID NO 49 <211> LENGTH: 21 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - DSP18.2 <400> SEQUENCE: 49 cugccuugug cacugcuuut t 21 <210> SEQ ID NO 50 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - DSP18.2 <400> SEQUENCE: 50 cugccuugug cacugcuuu 19 <210> SEQ ID NO 51 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - DSP18.2 <400> SEQUENCE: 51 aaagcagugc acaaggcag 19 <210> SEQ ID NO 52 <211> LENGTH: 21 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - DSP18.2 <220> FEATURE: <221> NAME/KEY: misc_feature <222> LOCATION: 20, 21 <223> OTHER INFORMATION: n = A,T,C,G or U <400> SEQUENCE: 52 cugccuugug cacugcuuun n 21 <210> SEQ ID NO 53 <211> LENGTH: 21 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - DSP18.2 <220> FEATURE: <221> NAME/KEY: misc_feature <222> LOCATION: 1, 2 <223> OTHER INFORMATION: n = A,T,C,G or U <400> SEQUENCE: 53 nnaaagcagu gcacaaggca g 21 <210> SEQ ID NO 54 <211> LENGTH: 21 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - DSP18.4 <400> SEQUENCE: 54 gaguuuggcu gggccaguut t 21 <210> SEQ ID NO 55 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - DSP18.4 <400> SEQUENCE: 55 gaguuuggcu gggccaguu 19 <210> SEQ ID NO 56 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - DSP18.4 <400> SEQUENCE: 56 aacuggccca gccaaacuc 19 <210> SEQ ID NO 57 <211> LENGTH: 21 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - DSP18.4 <220> FEATURE: <221> NAME/KEY: misc_feature <222> LOCATION: 20, 21 <223> OTHER INFORMATION: n = A,T,C,G or U <400> SEQUENCE: 57 gaguuuggcu gggccaguun n 21 <210> SEQ ID NO 58 <211> LENGTH: 21 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - DSP18.4 <220> FEATURE: <221> NAME/KEY: misc_feature <222> LOCATION: 1, 2 <223> OTHER INFORMATION: n = A,T,C,G or U <400> SEQUENCE: 58 nnaacuggcc cagccaaacu c 21 <210> SEQ ID NO 59 <211> LENGTH: 21 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - DSP13.1 <400> SEQUENCE: 59 cuugcgggaa uucaaggaat t 21 <210> SEQ ID NO 60 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - DSP13.1 <400> SEQUENCE: 60 cuugcgggaa uucaaggaa 19 <210> SEQ ID NO 61 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - DSP13.1 <400> SEQUENCE: 61 uuccuugaau ucccgcaag 19 <210> SEQ ID NO 62 <211> LENGTH: 21 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - DSP13.1 <220> FEATURE: <221> NAME/KEY: misc_feature <222> LOCATION: 20, 21 <223> OTHER INFORMATION: n = A,T,C,G or U <400> SEQUENCE: 62 cuugcgggaa uucaaggaan n 21 <210> SEQ ID NO 63 <211> LENGTH: 21 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - DSP13.1 <220> FEATURE: <221> NAME/KEY: misc_feature <222> LOCATION: 1, 2 <223> OTHER INFORMATION: n = A,T,C,G or U <400> SEQUENCE: 63 nnuuccuuga auucccgcaa g 21 <210> SEQ ID NO 64 <211> LENGTH: 21 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - DSP13.2 <400> SEQUENCE: 64 ccgaggggua cgguauauct t 21 <210> SEQ ID NO 65 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - DSP13.2 <400> SEQUENCE: 65 ccgaggggua cgguauauc 19 <210> SEQ ID NO 66 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - DSP13.2 <400> SEQUENCE: 66 gauauaccgu accccucgg 19 <210> SEQ ID NO 67 <211> LENGTH: 21 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - DSP13.2 <220> FEATURE: <221> NAME/KEY: misc_feature <222> LOCATION: 20, 21 <223> OTHER INFORMATION: n = A,T,C,G or U <400> SEQUENCE: 67 ccgaggggua cgguauaucn n 21 <210> SEQ ID NO 68 <211> LENGTH: 21 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - DSP13.2 <220> FEATURE: <221> NAME/KEY: misc_feature <222> LOCATION: 1, 2 <223> OTHER INFORMATION: n = A,T,C,G or U <400> SEQUENCE: 68 nngauauacc guaccccucg g 21 <210> SEQ ID NO 69 <211> LENGTH: 21 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - DSP13.3 <400> SEQUENCE: 69 caucaggcug gcuguaagat t 21 <210> SEQ ID NO 70 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - DSP13.3 <400> SEQUENCE: 70 caucaggcug gcuguaaga 19 <210> SEQ ID NO 71 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - DSP13.3 <400> SEQUENCE: 71 ucuuacagcc agccugaug 19 <210> SEQ ID NO 72 <211> LENGTH: 21 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - DSP13.3 <220> FEATURE: <221> NAME/KEY: misc_feature <222> LOCATION: 20, 21 <223> OTHER INFORMATION: n = A,T,C,G or U <400> SEQUENCE: 72 caucaggcug gcuguaagan n 21 <210> SEQ ID NO 73 <211> LENGTH: 21 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - DSP13.3 <220> FEATURE: <221> NAME/KEY: misc_feature <222> LOCATION: 1, 2 <223> OTHER INFORMATION: n = A,T,C,G or U <400> SEQUENCE: 73 nnucuuacag ccagccugau g 21 <210> SEQ ID NO 74 <211> LENGTH: 21 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - DSP13.4 <400> SEQUENCE: 74 cauggaucua aaugccuugt t 21 <210> SEQ ID NO 75 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - DSP13.4 <400> SEQUENCE: 75 cauggaucua aaugccuug 19 <210> SEQ ID NO 76 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - DSP13.4 <400> SEQUENCE: 76 caaggcauuu agauccaug 19 <210> SEQ ID NO 77 <211> LENGTH: 21 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - DSP13.4 <220> FEATURE: <221> NAME/KEY: misc_feature <222> LOCATION: 20, 21 <223> OTHER INFORMATION: n = A,T,C,G or U <400> SEQUENCE: 77 cauggaucua aaugccuugn n 21 <210> SEQ ID NO 78 <211> LENGTH: 21 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - DSP13.4 <220> FEATURE: <221> NAME/KEY: misc_feature <222> LOCATION: 1, 2 <223> OTHER INFORMATION: n = A,T,C,G or U <400> SEQUENCE: 78 nncaaggcau uuagauccau g 21 <210> SEQ ID NO 79 <211> LENGTH: 21 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - DSP14.1 <400> SEQUENCE: 79 gugaagacaa gccucaagat t 21 <210> SEQ ID NO 80 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - DSP14.1 <400> SEQUENCE: 80 gugaagacaa gccucaaga 19 <210> SEQ ID NO 81 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - DSP14.1 <400> SEQUENCE: 81 ucuugaggcu ugucuucac 19 <210> SEQ ID NO 82 <211> LENGTH: 21 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - DSP14.1 <220> FEATURE: <221> NAME/KEY: misc_feature <222> LOCATION: 20, 21 <223> OTHER INFORMATION: n = A,T,C,G or U <400> SEQUENCE: 82 gugaagacaa gccucaagan n 21 <210> SEQ ID NO 83 <211> LENGTH: 21 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - DSP14.1 <220> FEATURE: <221> NAME/KEY: misc_feature <222> LOCATION: 1, 2 <223> OTHER INFORMATION: n = A,T,C,G or U <400> SEQUENCE: 83 nnucuugagg cuugucuuca c 21 <210> SEQ ID NO 84 <211> LENGTH: 21 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - DSP14.2 <400> SEQUENCE: 84 gcucuacauu ggcgaugagt t 21 <210> SEQ ID NO 85 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - DSP14.2 <400> SEQUENCE: 85 gcucuacauu ggcgaugag 19 <210> SEQ ID NO 86 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - DSP14.2 <400> SEQUENCE: 86 cucaucgcca auguagagc 19 <210> SEQ ID NO 87 <211> LENGTH: 21 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - DSP14.2 <220> FEATURE: <221> NAME/KEY: misc_feature <222> LOCATION: 20, 21 <223> OTHER INFORMATION: n = A,T,C,G or U <400> SEQUENCE: 87 gcucuacauu ggcgaugagn n 21 <210> SEQ ID NO 88 <211> LENGTH: 21 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - DSP14.2 <220> FEATURE: <221> NAME/KEY: misc_feature <222> LOCATION: 1, 2 <223> OTHER INFORMATION: n = A,T,C,G or U <400> SEQUENCE: 88 nncucaucgc caauguagag c 21 <210> SEQ ID NO 89 <211> LENGTH: 21 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - DSP14.3 <400> SEQUENCE: 89 gcgacgacca caguaagaut t 21 <210> SEQ ID NO 90 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - DSP14.3 <400> SEQUENCE: 90 gcgacgacca caguaagau 19 <210> SEQ ID NO 91 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - DSP14.3 <400> SEQUENCE: 91 aucuuacugu ggucgucgc 19 <210> SEQ ID NO 92 <211> LENGTH: 21 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - DSP14.3 <220> FEATURE: <221> NAME/KEY: misc_feature <222> LOCATION: 20, 21 <223> OTHER INFORMATION: n = A,T,C,G or U <400> SEQUENCE: 92 gcgacgacca caguaagaun n 21 <210> SEQ ID NO 93 <211> LENGTH: 21 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - DSP14.3 <220> FEATURE: <221> NAME/KEY: misc_feature <222> LOCATION: 1, 2 <223> OTHER INFORMATION: n = A,T,C,G or U <400> SEQUENCE: 93 nnaucuuacu guggucgucg c 21 <210> SEQ ID NO 94 <211> LENGTH: 21 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - DSP14.4 <400> SEQUENCE: 94 ggacaugacc cugguggact t 21 <210> SEQ ID NO 95 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - DSP14.4 <400> SEQUENCE: 95 ggacaugacc cugguggac 19 <210> SEQ ID NO 96 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - DSP14.4 <400> SEQUENCE: 96 guccaccagg gucaugucc 19 <210> SEQ ID NO 97 <211> LENGTH: 21 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - DSP14.4 <220> FEATURE: <221> NAME/KEY: misc_feature <222> LOCATION: 20, 21 <223> OTHER INFORMATION: n = A,T,C,G or U <400> SEQUENCE: 97 ggacaugacc cugguggacn n 21 <210> SEQ ID NO 98 <211> LENGTH: 21 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - DSP14.4 <220> FEATURE: <221> NAME/KEY: misc_feature <222> LOCATION: 1, 2 <223> OTHER INFORMATION: n = A,T,C,G or U <400> SEQUENCE: 98 nnguccacca gggucauguc c 21 <210> SEQ ID NO 99 <211> LENGTH: 21 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - SHP2.1 <400> SEQUENCE: 99 gauucagaac acuggugaut t 21 <210> SEQ ID NO 100 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - SHP2.1 <400> SEQUENCE: 100 gauucagaac acuggugau 19 <210> SEQ ID NO 101 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - SHP2.1 <400> SEQUENCE: 101 aucaccagug uucugaauc 19 <210> SEQ ID NO 102 <211> LENGTH: 21 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - SHP2.1 <220> FEATURE: <221> NAME/KEY: misc_feature <222> LOCATION: 20, 21 <223> OTHER INFORMATION: n = A,T,C,G or U <400> SEQUENCE: 102 gauucagaac acuggugaun n 21 <210> SEQ ID NO 103 <211> LENGTH: 21 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - SHP2.1 <220> FEATURE: <221> NAME/KEY: misc_feature <222> LOCATION: 1, 2 <223> OTHER INFORMATION: n = A,T,C,G or U <400> SEQUENCE: 103 nnaucaccag uguucugaau c 21 <210> SEQ ID NO 104 <211> LENGTH: 21 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - SHP2.2 <400> SEQUENCE: 104 gaauauggcg ucaugcgugt t 21 <210> SEQ ID NO 105 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - SHP2.2 <400> SEQUENCE: 105 gaauauggcg ucaugcgug 19 <210> SEQ ID NO 106 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - SHP2.2 <400> SEQUENCE: 106 cacgcaugac gccauauuc 19 <210> SEQ ID NO 107 <211> LENGTH: 21 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - SHP2.2 <220> FEATURE: <221> NAME/KEY: misc_feature <222> LOCATION: 20, 21 <223> OTHER INFORMATION: n = A,T,C,G or U <400> SEQUENCE: 107 gaauauggcg ucaugcgugn n 21 <210> SEQ ID NO 108 <211> LENGTH: 21 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - SHP2.2 <220> FEATURE: <221> NAME/KEY: misc_feature <222> LOCATION: 1, 2 <223> OTHER INFORMATION: n = A,T,C,G or U <400> SEQUENCE: 108 nncacgcaug acgccauauu c 21 <210> SEQ ID NO 109 <211> LENGTH: 21 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - SHP2.3 <400> SEQUENCE: 109 cggucuggca auaccacuut t 21 <210> SEQ ID NO 110 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - SHP2.3 <400> SEQUENCE: 110 cggucuggca auaccacuu 19 <210> SEQ ID NO 111 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - SHP2.3 <400> SEQUENCE: 111 aagugguauu gccagaccg 19 <210> SEQ ID NO 112 <211> LENGTH: 21 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - SHP2.3 <220> FEATURE: <221> NAME/KEY: misc_feature <222> LOCATION: 20, 21 <223> OTHER INFORMATION: n = A,T,C,G or U <400> SEQUENCE: 112 cggucuggca auaccacuun n 21 <210> SEQ ID NO 113 <211> LENGTH: 21 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - SHP2.3 <220> FEATURE: <221> NAME/KEY: misc_feature <222> LOCATION: 1, 2 <223> OTHER INFORMATION: n = A,T,C,G or U <400> SEQUENCE: 113 nnaaguggua uugccagacc g 21 <210> SEQ ID NO 114 <211> LENGTH: 21 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - SHP2.4 <400> SEQUENCE: 114 ugacggcaag ucuaaagugt t 21 <210> SEQ ID NO 115 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - SHP2.4 <400> SEQUENCE: 115 ugacggcaag ucuaaagug 19 <210> SEQ ID NO 116 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - SHP2.4 <400> SEQUENCE: 116 cacuuuagac uugccguca 19 <210> SEQ ID NO 117 <211> LENGTH: 21 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - SHP2.4 <220> FEATURE: <221> NAME/KEY: misc_feature <222> LOCATION: 20, 21 <223> OTHER INFORMATION: n = A,T,C,G or U <400> SEQUENCE: 117 ugacggcaag ucuaaagugn n 21 <210> SEQ ID NO 118 <211> LENGTH: 21 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - SHP2.4 <220> FEATURE: <221> NAME/KEY: misc_feature <222> LOCATION: 1, 2 <223> OTHER INFORMATION: n = A,T,C,G or U <400> SEQUENCE: 118 nncacuuuag acuugccguc a 21 <210> SEQ ID NO 119 <211> LENGTH: 21 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - KAP.1 <400> SEQUENCE: 119 gagccuauug aagaugaact t 21 <210> SEQ ID NO 120 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - KAP.1 <400> SEQUENCE: 120 gagccuauug aagaugaac 19 <210> SEQ ID NO 121 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - KAP.1 <400> SEQUENCE: 121 guucaucuuc aauaggcuc 19 <210> SEQ ID NO 122 <211> LENGTH: 21 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - KAP.1 <220> FEATURE: <221> NAME/KEY: misc_feature <222> LOCATION: 20, 21 <223> OTHER INFORMATION: n = A,T,C,G or U <400> SEQUENCE: 122 gagccuauug aagaugaacn n 21 <210> SEQ ID NO 123 <211> LENGTH: 21 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - KAP.1 <220> FEATURE: <221> NAME/KEY: misc_feature <222> LOCATION: 1, 2 <223> OTHER INFORMATION: n = A,T,C,G or U <400> SEQUENCE: 123 nnguucaucu ucaauaggcu c 21 <210> SEQ ID NO 124 <211> LENGTH: 21 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - KAP.2 <400> SEQUENCE: 124 gagcuguggu auacaagact t 21 <210> SEQ ID NO 125 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - KAP.2 <400> SEQUENCE: 125 gagcuguggu auacaagac 19 <210> SEQ ID NO 126 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - KAP.2 <400> SEQUENCE: 126 gucuuguaua ccacagcuc 19 <210> SEQ ID NO 127 <211> LENGTH: 21 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - KAP.2 <220> FEATURE: <221> NAME/KEY: misc_feature <222> LOCATION: 20, 21 <223> OTHER INFORMATION: n = A,T,C,G or U <400> SEQUENCE: 127 gagcuguggu auacaagacn n 21 <210> SEQ ID NO 128 <211> LENGTH: 21 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - KAP.2 <220> FEATURE: <221> NAME/KEY: misc_feature <222> LOCATION: 1, 2 <223> OTHER INFORMATION: n = A,T,C,G or U <400> SEQUENCE: 128 nngucuugua uaccacagcu c 21 <210> SEQ ID NO 129 <211> LENGTH: 21 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - KAP.3 <400> SEQUENCE: 129 gagcuuacaa ccugccuuat t 21 <210> SEQ ID NO 130 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - KAP.3 <400> SEQUENCE: 130 gagcuuacaa ccugccuua 19 <210> SEQ ID NO 131 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - KAP.3 <400> SEQUENCE: 131 uaaggcaggu uguaagcuc 19 <210> SEQ ID NO 132 <211> LENGTH: 21 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - KAP.3 <220> FEATURE: <221> NAME/KEY: misc_feature <222> LOCATION: 20, 21 <223> OTHER INFORMATION: n = A,T,C,G or U <400> SEQUENCE: 132 gagcuuacaa ccugccuuan n 21 <210> SEQ ID NO 133 <211> LENGTH: 21 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - KAP.3 <220> FEATURE: <221> NAME/KEY: misc_feature <222> LOCATION: 1, 2 <223> OTHER INFORMATION: n = A,T,C,G or U <400> SEQUENCE: 133 nnuaaggcag guuguaagcu c 21 <210> SEQ ID NO 134 <211> LENGTH: 21 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - KAP.4 <400> SEQUENCE: 134 uacacugcua uggaggacut t 21 <210> SEQ ID NO 135 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - KAP.4 <400> SEQUENCE: 135 uacacugcua uggaggacu 19 <210> SEQ ID NO 136 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - KAP.4 <400> SEQUENCE: 136 aguccuccau agcagugua 19 <210> SEQ ID NO 137 <211> LENGTH: 21 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - KAP.4 <220> FEATURE: <221> NAME/KEY: misc_feature <222> LOCATION: 20, 21 <223> OTHER INFORMATION: n = A,T,C,G or U <400> SEQUENCE: 137 uacacugcua uggaggacun n 21 <210> SEQ ID NO 138 <211> LENGTH: 21 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - KAP.4 <220> FEATURE: <221> NAME/KEY: misc_feature <222> LOCATION: 1, 2 <223> OTHER INFORMATION: n = A,T,C,G or U <400> SEQUENCE: 138 nnaguccucc auagcagugu a 21 <210> SEQ ID NO 139 <211> LENGTH: 21 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - Prl3.1 <400> SEQUENCE: 139 gugaccuaug acaaaacgct t 21 <210> SEQ ID NO 140 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - Prl3.1 <400> SEQUENCE: 140 gugaccuaug acaaaacgc 19 <210> SEQ ID NO 141 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - Prl3.1 <400> SEQUENCE: 141 gcguuuuguc auaggucac 19 <210> SEQ ID NO 142 <211> LENGTH: 21 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - Prl3.1 <220> FEATURE: <221> NAME/KEY: misc_feature <222> LOCATION: 20, 21 <223> OTHER INFORMATION: n = A,T,C,G or U <400> SEQUENCE: 142 gugaccuaug acaaaacgcn n 21 <210> SEQ ID NO 143 <211> LENGTH: 21 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - Prl3.1 <220> FEATURE: <221> NAME/KEY: misc_feature <222> LOCATION: 1, 2 <223> OTHER INFORMATION: n = A,T,C,G or U <400> SEQUENCE: 143 nngcguuuug ucauagguca c 21 <210> SEQ ID NO 144 <211> LENGTH: 21 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - Prl3.2 <400> SEQUENCE: 144 ggccaaguuc ugugaggcct t 21 <210> SEQ ID NO 145 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - Prl3.2 <400> SEQUENCE: 145 ggccaaguuc ugugaggcc 19 <210> SEQ ID NO 146 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - Prl3.2 <400> SEQUENCE: 146 ggccucacag aacuuggcc 19 <210> SEQ ID NO 147 <211> LENGTH: 21 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - Prl3.2 <220> FEATURE: <221> NAME/KEY: misc_feature <222> LOCATION: 20, 21 <223> OTHER INFORMATION: n = A,T,C,G or U <400> SEQUENCE: 147 ggccaaguuc ugugaggccn n 21 <210> SEQ ID NO 148 <211> LENGTH: 21 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - Prl3.2 <220> FEATURE: <221> NAME/KEY: misc_feature <222> LOCATION: 1, 2 <223> OTHER INFORMATION: n = A,T,C,G or U <400> SEQUENCE: 148 nnggccucac agaacuuggc c 21 <210> SEQ ID NO 149 <211> LENGTH: 21 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - Prl3.3 <400> SEQUENCE: 149 guacgaggac gccauccagt t 21 <210> SEQ ID NO 150 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - Prl3.3 <400> SEQUENCE: 150 guacgaggac gccauccag 19 <210> SEQ ID NO 151 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - Prl3.3 <400> SEQUENCE: 151 cuggauggcg uccucguac 19 <210> SEQ ID NO 152 <211> LENGTH: 21 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - Prl3.3 <220> FEATURE: <221> NAME/KEY: misc_feature <222> LOCATION: 20, 21 <223> OTHER INFORMATION: n = A,T,C,G or U <400> SEQUENCE: 152 guacgaggac gccauccagn n 21 <210> SEQ ID NO 153 <211> LENGTH: 21 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - Prl3.3 <220> FEATURE: <221> NAME/KEY: misc_feature <222> LOCATION: 1, 2 <223> OTHER INFORMATION: n = A,T,C,G or U <400> SEQUENCE: 153 nncuggaugg cguccucgua c 21 <210> SEQ ID NO 154 <211> LENGTH: 21 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - Prl3.4 <400> SEQUENCE: 154 uaccggccca aacagaggct t 21 <210> SEQ ID NO 155 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - Prl3.4 <400> SEQUENCE: 155 uaccggccca aacagaggc 19 <210> SEQ ID NO 156 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - Prl3.4 <400> SEQUENCE: 156 gccucuguuu gggccggua 19 <210> SEQ ID NO 157 <211> LENGTH: 21 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - Prl3.4 <220> FEATURE: <221> NAME/KEY: misc_feature <222> LOCATION: 20, 21 <223> OTHER INFORMATION: n = A,T,C,G or U <400> SEQUENCE: 157 uaccggccca aacagaggcn n 21 <210> SEQ ID NO 158 <211> LENGTH: 21 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - Prl3.4 <220> FEATURE: <221> NAME/KEY: misc_feature <222> LOCATION: 1, 2 <223> OTHER INFORMATION: n = A,T,C,G or U <400> SEQUENCE: 158 nngccucugu uugggccggu a 21 <210> SEQ ID NO 159 <211> LENGTH: 21 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - RPTPE.1 <400> SEQUENCE: 159 gcagaggaaa gcugugguct t 21 <210> SEQ ID NO 160 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - RPTPE.1 <400> SEQUENCE: 160 gcagaggaaa gcugugguc 19 <210> SEQ ID NO 161 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - RPTPE.1 <400> SEQUENCE: 161 gaccacagcu uuccucugc 19 <210> SEQ ID NO 162 <211> LENGTH: 21 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - RPTPE.1 <220> FEATURE: <221> NAME/KEY: misc_feature <222> LOCATION: 20, 21 <223> OTHER INFORMATION: n = A,T,C,G or U <400> SEQUENCE: 162 gcagaggaaa gcuguggucn n 21 <210> SEQ ID NO 163 <211> LENGTH: 21 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - RPTPE.1 <220> FEATURE: <221> NAME/KEY: misc_feature <222> LOCATION: 1, 2 <223> OTHER INFORMATION: n = A,T,C,G or U <400> SEQUENCE: 163 nngaccacag cuuuccucug c 21 <210> SEQ ID NO 164 <211> LENGTH: 21 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - RPTPE.2 <400> SEQUENCE: 164 gucugcgacc aucgucaugt t 21 <210> SEQ ID NO 165 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - RPTPE.2 <400> SEQUENCE: 165 gucugcgacc aucgucaug 19 <210> SEQ ID NO 166 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - RPTPE.2 <400> SEQUENCE: 166 caugacgaug gucgcagac 19 <210> SEQ ID NO 167 <211> LENGTH: 21 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - RPTPE.2 <220> FEATURE: <221> NAME/KEY: misc_feature <222> LOCATION: 20, 21 <223> OTHER INFORMATION: n = A,T,C,G or U <400> SEQUENCE: 167 gucugcgacc aucgucaugn n 21 <210> SEQ ID NO 168 <211> LENGTH: 21 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - RPTPE.2 <220> FEATURE: <221> NAME/KEY: misc_feature <222> LOCATION: 1, 2 <223> OTHER INFORMATION: n = A,T,C,G or U <400> SEQUENCE: 168 nncaugacga uggucgcaga c 21 <210> SEQ ID NO 169 <211> LENGTH: 21 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - RPTPE.3 <400> SEQUENCE: 169 gccuuacucg aguacuacct t 21 <210> SEQ ID NO 170 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - RPTPE.3 <400> SEQUENCE: 170 gccuuacucg aguacuacc 19 <210> SEQ ID NO 171 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - RPTPE.3 <400> SEQUENCE: 171 gguaguacuc gaguaaggc 19 <210> SEQ ID NO 172 <211> LENGTH: 21 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - RPTPE.3 <220> FEATURE: <221> NAME/KEY: misc_feature <222> LOCATION: 20, 21 <223> OTHER INFORMATION: n = A,T,C,G or U <400> SEQUENCE: 172 gccuuacucg aguacuaccn n 21 <210> SEQ ID NO 173 <211> LENGTH: 21 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - RPTPE.3 <220> FEATURE: <221> NAME/KEY: misc_feature <222> LOCATION: 1, 2 <223> OTHER INFORMATION: n = A,T,C,G or U <400> SEQUENCE: 173 nngguaguac ucgaguaagg c 21 <210> SEQ ID NO 174 <211> LENGTH: 21 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - RPTPE.4 <400> SEQUENCE: 174 ggacuauuuc aucgccacct t 21 <210> SEQ ID NO 175 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - RPTPE.4 <400> SEQUENCE: 175 ggacuauuuc aucgccacc 19 <210> SEQ ID NO 176 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - RPTPE.4 <400> SEQUENCE: 176 gguggcgaug aaauagucc 19 <210> SEQ ID NO 177 <211> LENGTH: 21 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - RPTPE.4 <220> FEATURE: <221> NAME/KEY: misc_feature <222> LOCATION: 20, 21 <223> OTHER INFORMATION: n = A,T,C,G or U <400> SEQUENCE: 177 ggacuauuuc aucgccaccn n 21 <210> SEQ ID NO 178 <211> LENGTH: 21 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - RPTPE.4 <220> FEATURE: <221> NAME/KEY: misc_feature <222> LOCATION: 1, 2 <223> OTHER INFORMATION: n = A,T,C,G or U <400> SEQUENCE: 178 nngguggcga ugaaauaguc c 21 <210> SEQ ID NO 179 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA <400> SEQUENCE: 179 ccaccaucac agcgaacac 19 <210> SEQ ID NO 180 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA <400> SEQUENCE: 180 agcgcuguca uuucaacca 19 <210> SEQ ID NO 181 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA <400> SEQUENCE: 181 accacaacaa uagcuacua 19 <210> SEQ ID NO 182 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA <400> SEQUENCE: 182 gcuacuacuc caucuaagc 19 <210> SEQ ID NO 183 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA <400> SEQUENCE: 183 aaugcgucug uuuccauau 19 <210> SEQ ID NO 184 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA <400> SEQUENCE: 184 augcgucugu uuccauauc 19 <210> SEQ ID NO 185 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA <400> SEQUENCE: 185 ugcgucuguu uccauaucu 19 <210> SEQ ID NO 186 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA <400> SEQUENCE: 186 accuuuacuu gugauacac 19 <210> SEQ ID NO 187 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA <400> SEQUENCE: 187 cagauuucag ugugguaau 19 <210> SEQ ID NO 188 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA <400> SEQUENCE: 188 acccgaacau gaguauaag 19 <210> SEQ ID NO 189 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA <400> SEQUENCE: 189 cccgaacaug aguauaagu 19 <210> SEQ ID NO 190 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA <400> SEQUENCE: 190 caaguuuacu aacgcaagu 19 <210> SEQ ID NO 191 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA <400> SEQUENCE: 191 ggaguaauua ccuggaauc 19 <210> SEQ ID NO 192 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA <400> SEQUENCE: 192 caugccuaca ucauugcaa 19 <210> SEQ ID NO 193 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA <400> SEQUENCE: 193 auaguaugca ugucaagug 19 <210> SEQ ID NO 194 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA <400> SEQUENCE: 194 ugaacguuac cauuuggaa 19 <210> SEQ ID NO 195 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA <400> SEQUENCE: 195 augagucgca uaagaauug 19 <210> SEQ ID NO 196 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA <400> SEQUENCE: 196 ugagucgcau aagaauugc 19 <210> SEQ ID NO 197 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA <400> SEQUENCE: 197 gaauugcgau uuccgugua 19 <210> SEQ ID NO 198 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA <400> SEQUENCE: 198 auugcgauuu ccguguaaa 19 <210> SEQ ID NO 199 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA <400> SEQUENCE: 199 gccaauccau gcagauauu 19 <210> SEQ ID NO 200 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA <400> SEQUENCE: 200 uuauaaccgu guugaacuc 19 <210> SEQ ID NO 201 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA <400> SEQUENCE: 201 uaaccguguu gaacucucu 19 <210> SEQ ID NO 202 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA <400> SEQUENCE: 202 acggagaugc agggucaaa 19 <210> SEQ ID NO 203 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA <400> SEQUENCE: 203 gaugcagggu caaacuaca 19 <210> SEQ ID NO 204 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA <400> SEQUENCE: 204 acccaggaaa uacauugcu 19 <210> SEQ ID NO 205 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA <400> SEQUENCE: 205 uguccagauu acaucauuc 19 <210> SEQ ID NO 206 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA <400> SEQUENCE: 206 augccuucag caauuucuu 19 <210> SEQ ID NO 207 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA <400> SEQUENCE: 207 caggaaccua uaucggaau 19 <210> SEQ ID NO 208 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA <400> SEQUENCE: 208 ggaaccuaua ucggaauug 19 <210> SEQ ID NO 209 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA <400> SEQUENCE: 209 accuauaucg gaauugaug 19 <210> SEQ ID NO 210 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA <400> SEQUENCE: 210 guggauguuu augguuaug 19 <210> SEQ ID NO 211 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA <400> SEQUENCE: 211 ggcgacagag augccugau 19 <210> SEQ ID NO 212 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA <400> SEQUENCE: 212 gaggcccagu acaucuuga 19 <210> SEQ ID NO 213 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA <400> SEQUENCE: 213 ggcccaguac aucuugauc 19 <210> SEQ ID NO 214 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA <400> SEQUENCE: 214 gcuacuggaa accugaagu 19 <210> SEQ ID NO 215 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA <400> SEQUENCE: 215 accugaagug augauugcu 19 <210> SEQ ID NO 216 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA <400> SEQUENCE: 216 aguugaccug aaagacaca 19 <210> SEQ ID NO 217 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA <400> SEQUENCE: 217 acuuauaccc uucgugucu 19 <210> SEQ ID NO 218 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA <400> SEQUENCE: 218 cuuauacccu ucgugucuu 19 <210> SEQ ID NO 219 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA <400> SEQUENCE: 219 ggaaagacuc ucgaacugu 19 <210> SEQ ID NO 220 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA <400> SEQUENCE: 220 acccaaggaa uuaaucucu 19 <210> SEQ ID NO 221 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA <400> SEQUENCE: 221 cccaaggaau uaaucucua 19 <210> SEQ ID NO 222 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA <400> SEQUENCE: 222 ugauucaggu cgucaaaca 19 <210> SEQ ID NO 223 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA <400> SEQUENCE: 223 gggauggauc ucagcaaac 19 <210> SEQ ID NO 224 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA <400> SEQUENCE: 224 ucucagcaaa cgggaauau 19 <210> SEQ ID NO 225 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA <400> SEQUENCE: 225 uucgagcaau aucaauucc 19 <210> SEQ ID NO 226 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA <400> SEQUENCE: 226 ccuacccugc ucagaaugg 19 <210> SEQ ID NO 227 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA <400> SEQUENCE: 227 auggagcugu cacccacau 19 <210> SEQ ID NO 228 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA <400> SEQUENCE: 228 uggaacauca cgggcaauu 19 <210> SEQ ID NO 229 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA <400> SEQUENCE: 229 gcaaugacgg caagucuaa 19 SEQ ID NO 2 30 <211> LENGTH: 19 <212> TYPE: RNA ORGANISM: Artificial Sequen ce <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA <400> SEQUENCE: 230 augacggcaa gucuaaagu 19 <210> SEQ ID NO 231 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA <400> SEQUENCE: 231 ugacggcaag ucuaaagug 19 <210> SEQ ID NO 232 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA <400> SEQUENCE: 232 gucuaaagug acccauguu 19 <210> SEQ ID NO 233 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA <400> SEQUENCE: 233 ugauucgcug ucaggaacu 19 <210> SEQ ID NO 234 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA <400> SEQUENCE: 234 cgacguuggu ggaggagaa 19 <210> SEQ ID NO 235 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA <400> SEQUENCE: 235 acgguuugau ucuuugaca 19 <210> SEQ ID NO 236 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA <400> SEQUENCE: 236 uucuuugaca gaucuugug 19 <210> SEQ ID NO 237 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA <400> SEQUENCE: 237 gaauccuaug guggaaaca 19 <210> SEQ ID NO 238 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA <400> SEQUENCE: 238 auccuauggu ggaaacauu 19 <210> SEQ ID NO 239 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA <400> SEQUENCE: 239 uccuauggug gaaacauug 19 <210> SEQ ID NO 240 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA <400> SEQUENCE: 240 caguacuaca acucaagca 19 <210> SEQ ID NO 241 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA <400> SEQUENCE: 241 uuugagacac uacaacaac 19 <210> SEQ ID NO 242 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA <400> SEQUENCE: 242 aacuucucua cagccgaaa 19 <210> SEQ ID NO 243 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA <400> SEQUENCE: 243 acauccugcc cuuugauca 19 <210> SEQ ID NO 244 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA <400> SEQUENCE: 244 ucauaccagg guuguccua 19 <210> SEQ ID NO 245 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA <400> SEQUENCE: 245 uaccaggguu guccuacac 19 <210> SEQ ID NO 246 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA <400> SEQUENCE: 246 uuugaaacca agugcaaca 19 <210> SEQ ID NO 247 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA <400> SEQUENCE: 247 agaguuacau ugccacaca 19 <210> SEQ ID NO 248 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA <400> SEQUENCE: 248 gaguuacauu gccacacaa 19 <210> SEQ ID NO 249 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA <400> SEQUENCE: 249 aaacacggug aaugacuuu 19 <210> SEQ ID NO 250 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA <400> SEQUENCE: 250 cuggccugau gaguaugcu 19 <210> SEQ ID NO 251 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA <400> SEQUENCE: 251 uggcgucaug cguguuagg 19 <210> SEQ ID NO 252 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA <400> SEQUENCE: 252 ugcguguuag gaacgucaa 19 <210> SEQ ID NO 253 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA <400> SEQUENCE: 253 ugacuauacg cuaagagaa 19 <210> SEQ ID NO 254 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA <400> SEQUENCE: 254 cuauacgcua agagaacuu 19 <210> SEQ ID NO 255 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA <400> SEQUENCE: 255 gguuggacaa gggaauacg 19 <210> SEQ ID NO 256 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA <400> SEQUENCE: 256 gaacggucug gcaauacca 19 <210> SEQ ID NO 257 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA <400> SEQUENCE: 257 cggucuggca auaccacuu 19 <210> SEQ ID NO 258 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA <400> SEQUENCE: 258 aagguguuga cugcgauau 19 <210> SEQ ID NO 259 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA <400> SEQUENCE: 259 agguguugac ugcgauauu 19 <210> SEQ ID NO 260 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA <400> SEQUENCE: 260 gguguugacu gcgauauug 19 <210> SEQ ID NO 261 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA <400> SEQUENCE: 261 uauggcgguc cagcauuau 19 <210> SEQ ID NO 262 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA <400> SEQUENCE: 262 uggcggucca gcauuauau 19 <210> SEQ ID NO 263 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA <400> SEQUENCE: 263 aacacuacag cgcaggauu 19 <210> SEQ ID NO 264 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA <400> SEQUENCE: 264 acacuacagc gcaggauug 19 <210> SEQ ID NO 265 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA <400> SEQUENCE: 265 gcgcaggauu gaagaagag 19 <210> SEQ ID NO 266 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA <400> SEQUENCE: 266 gaggaaaggg cacgaauau 19 <210> SEQ ID NO 267 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA <400> SEQUENCE: 267 ggaaagggca cgaauauac 19 <210> SEQ ID NO 268 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA <400> SEQUENCE: 268 gggcacgaau auacaaaua 19 <210> SEQ ID NO 269 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA <400> SEQUENCE: 269 aaacgugggc cugaugcaa 19 <210> SEQ ID NO 270 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA <400> SEQUENCE: 270 acgugggccu gaugcaaca 19 <210> SEQ ID NO 271 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA <400> SEQUENCE: 271 gcacaguaaa uacccacua 19 <210> SEQ ID NO 272 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA <400> SEQUENCE: 272 cuauuucucc aucgaugag 19 <210> SEQ ID NO 273 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA <400> SEQUENCE: 273 acuuggcaau gguguacag 19 <210> SEQ ID NO 274 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA <400> SEQUENCE: 274 ggugccuaug caguaaucu 19 <210> SEQ ID NO 275 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA <400> SEQUENCE: 275 ucucaccauu cucgacugu 19 <210> SEQ ID NO 276 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA <400> SEQUENCE: 276 aagggauuac aacauggau 19 <210> SEQ ID NO 277 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA <400> SEQUENCE: 277 agggauuaca acauggauu 19 <210> SEQ ID NO 278 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA <400> SEQUENCE: 278 gggauuacaa cauggauuu 19 <210> SEQ ID NO 279 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA <400> SEQUENCE: 279 gaaugguuau ccucuucac 19 <210> SEQ ID NO 280 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA <400> SEQUENCE: 280 gcauaaugug acugcaguu 19 <210> SEQ ID NO 281 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA <400> SEQUENCE: 281 cgcuggcuuc gagcacuau 19 <210> SEQ ID NO 282 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA <400> SEQUENCE: 282 gcacacccag ugacaacau 19 <210> SEQ ID NO 283 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA <400> SEQUENCE: 283 acaucgugcg aagguuccu 19 <210> SEQ ID NO 284 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA <400> SEQUENCE: 284 agaacaggga cauugauag 19 <210> SEQ ID NO 285 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA <400> SEQUENCE: 285 gaacagggac auugauagc 19 <210> SEQ ID NO 286 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA <400> SEQUENCE: 286 gggacauuga uagccuguu 19 <210> SEQ ID NO 287 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA <400> SEQUENCE: 287 cauugauagc cuguuaugu 19 <210> SEQ ID NO 288 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA <400> SEQUENCE: 288 cuacagguuu acacaugcu 19 <210> SEQ ID NO 289 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA <400> SEQUENCE: 289 aaaucgacca uccagugaa 19 <210> SEQ ID NO 290 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA <400> SEQUENCE: 290 aaucgaccau ccagugaag 19 <210> SEQ ID NO 291 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA <400> SEQUENCE: 291 ucgaccaucc agugaagga 19 <210> SEQ ID NO 292 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA <400> SEQUENCE: 292 aaauucuuuc uggccuaga 19 <210> SEQ ID NO 293 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA <400> SEQUENCE: 293 ugucuauugg uggaaaucu 19 <210> SEQ ID NO 294 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA <400> SEQUENCE: 294 acgauuugga gagguaagu 19 <210> SEQ ID NO 295 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA <400> SEQUENCE: 295 cgauuuggag agguaaguu 19 <210> SEQ ID NO 296 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA <400> SEQUENCE: 296 gagacauccu auauuccuu 19 <210> SEQ ID NO 297 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA <400> SEQUENCE: 297 auaccagacc gauuuauug 19 <210> SEQ ID NO 298 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA <400> SEQUENCE: 298 uaccagaccg auuuauugc 19 <210> SEQ ID NO 299 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA <400> SEQUENCE: 299 gaccgauuua uugccuucu 19 <210> SEQ ID NO 300 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA <400> SEQUENCE: 300 aaggauguau gaugccaaa 19 <210> SEQ ID NO 301 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA <400> SEQUENCE: 301 aggauguaug augccaaac 19 <210> SEQ ID NO 302 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA <400> SEQUENCE: 302 ggauguauga ugccaaacg 19 <210> SEQ ID NO 303 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA <400> SEQUENCE: 303 cggaugcugg cuucgauca 19 <210> SEQ ID NO 304 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA <400> SEQUENCE: 304 ugccauuguc aaagaauuc 19 <210> SEQ ID NO 305 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA <400> SEQUENCE: 305 gggugccauu gcaguacau 19 <210> SEQ ID NO 306 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA <400> SEQUENCE: 306 gaccuggcuc ggugauugg 19 <210> SEQ ID NO 307 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA <400> SEQUENCE: 307 cccgaaccgu acagugaug 19 <210> SEQ ID NO 308 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA <400> SEQUENCE: 308 accguacagu gaugaugac 19 <210> SEQ ID NO 309 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA <400> SEQUENCE: 309 uagacuucgg gccuugaaa 19 <210> SEQ ID NO 310 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA <400> SEQUENCE: 310 acaaacgcua uuccucuca 19 <210> SEQ ID NO 311 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA <400> SEQUENCE: 311 gggucugggc agugauuau 19 <210> SEQ ID NO 312 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA <400> SEQUENCE: 312 gcaaccacug gaggugaag 19 <210> SEQ ID NO 313 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA <400> SEQUENCE: 313 auccuaugag aagaauaca 19 <210> SEQ ID NO 314 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA <400> SEQUENCE: 314 uccuaugaga agaauacau 19 <210> SEQ ID NO 315 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA <400> SEQUENCE: 315 aaagcuguug ggauguagu 19 <210> SEQ ID NO 316 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA <400> SEQUENCE: 316 uucugauucu cuugaccau 19 <210> SEQ ID NO 317 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA <400> SEQUENCE: 317 gaagccagua agaccugua 19 <210> SEQ ID NO 318 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA <400> SEQUENCE: 318 cagccacuuu gucugauga 19 <210> SEQ ID NO 319 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA <400> SEQUENCE: 319 aaccuugaca accgaugca 19 <210> SEQ ID NO 320 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA <400> SEQUENCE: 320 caaccgaugc aagcuguuu 19 <210> SEQ ID NO 321 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA <400> SEQUENCE: 321 accgaugcaa gcuguuuga 19 <210> SEQ ID NO 322 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA <400> SEQUENCE: 322 cucggucagu guugaagag 19 <210> SEQ ID NO 323 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA <400> SEQUENCE: 323 acguucucaa gaggagucu 19 <210> SEQ ID NO 324 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA <400> SEQUENCE: 324 gucaacuaau ccagagaag 19 <210> SEQ ID NO 325 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA <400> SEQUENCE: 325 aggcccauga gacucuuca 19 <210> SEQ ID NO 326 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA <400> SEQUENCE: 326 agggaccuua uaggagacu 19 <210> SEQ ID NO 327 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA <400> SEQUENCE: 327 gggaccuuau aggagacuu 19 <210> SEQ ID NO 328 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA <400> SEQUENCE: 328 gacuucucca aggguuauc 19 <210> SEQ ID NO 329 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA <400> SEQUENCE: 329 guuuguuauc aucgacugu 19 <210> SEQ ID NO 330 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA <400> SEQUENCE: 330 cugucgauac ccauaugaa 19 <210> SEQ ID NO 331 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA <400> SEQUENCE: 331 gaagcccauu guaccuacu 19 <210> SEQ ID NO 332 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA <400> SEQUENCE: 332 agcccauugu accuacuga 19 <210> SEQ ID NO 333 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA <400> SEQUENCE: 333 gcccauugua ccuacugau 19 <210> SEQ ID NO 334 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA <400> SEQUENCE: 334 uggcaagcgu gucauuguu 19 <210> SEQ ID NO 335 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA <400> SEQUENCE: 335 agcgugucau uguuguguu 19 <210> SEQ ID NO 336 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA <400> SEQUENCE: 336 ugugccggua ugugagaga 19 <210> SEQ ID NO 337 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA <400> SEQUENCE: 337 gagagaucgc cuggguaau 19 <210> SEQ ID NO 338 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA <400> SEQUENCE: 338 gagaucgccu ggguaauga 19 <210> SEQ ID NO 339 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA <400> SEQUENCE: 339 gaucgccugg guaaugaau 19 <210> SEQ ID NO 340 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA <400> SEQUENCE: 340 auccucccug ucgucugaa 19 <210> SEQ ID NO 341 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA <400> SEQUENCE: 341 uccucccugu cgucugaau 19 <210> SEQ ID NO 342 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA <400> SEQUENCE: 342 uggcggagca gacguuuga 19 <210> SEQ ID NO 343 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA <400> SEQUENCE: 343 cguuugaaca ggccaucca 19 <210> SEQ ID NO 344 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA <400> SEQUENCE: 344 gccggaucau ucgaaacga 19 <210> SEQ ID NO 345 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA <400> SEQUENCE: 345 ucauucgaaa cgagcaguu 19 <210> SEQ ID NO 346 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA <400> SEQUENCE: 346 gucuaugccg gauggauuu 19 <210> SEQ ID NO 347 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA <400> SEQUENCE: 347 ugccggaugg auuugucuu 19 <210> SEQ ID NO 348 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA <400> SEQUENCE: 348 aaaggaccuc gucauguac 19 <210> SEQ ID NO 349 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA <400> SEQUENCE: 349 aaucacugug ucacgauga 19 <210> SEQ ID NO 350 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA <400> SEQUENCE: 350 aucacugugu cacgaugag 19 <210> SEQ ID NO 351 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA <400> SEQUENCE: 351 gagcugauug gagauuacu 19 <210> SEQ ID NO 352 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA <400> SEQUENCE: 352 gcugauugga gauuacucu 19 <210> SEQ ID NO 353 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA <400> SEQUENCE: 353 cucuaaggcc uuccuccua 19 <210> SEQ ID NO 354 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA <400> SEQUENCE: 354 cagacaguag acggaaagc 19 <210> SEQ ID NO 355 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA <400> SEQUENCE: 355 agcaccaaga ccucaagua 19 <210> SEQ ID NO 356 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA <400> SEQUENCE: 356 gaaacgaugg uggcccuau 19 <210> SEQ ID NO 357 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA <400> SEQUENCE: 357 aacgauggug gcccuauug 19 <210> SEQ ID NO 358 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA <400> SEQUENCE: 358 cgccgagagc uuccuacug 19 <210> SEQ ID NO 359 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA <400> SEQUENCE: 359 gaacuccagu gggcaaauu 19 <210> SEQ ID NO 360 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA <400> SEQUENCE: 360 uuuagcuggg augacaaug 19 <210> SEQ ID NO 361 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA <400> SEQUENCE: 361 uucaaggaca acacaauac 19 <210> SEQ ID NO 362 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA <400> SEQUENCE: 362 acacaauacc agauaaagu 19 <210> SEQ ID NO 363 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA <400> SEQUENCE: 363 cacaauacca gauaaaguu 19 <210> SEQ ID NO 364 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA <400> SEQUENCE: 364 ggaagggcuu auguuuaaa 19 <210> SEQ ID NO 365 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA <400> SEQUENCE: 365 caccaagauc ugaaguaug 19 <210> SEQ ID NO 366 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA <400> SEQUENCE: 366 aguaugucaa cccagaaac 19 <210> SEQ ID NO 367 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA <400> SEQUENCE: 367 guaugucaac ccagaaaca 19 <210> SEQ ID NO 368 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA <400> SEQUENCE: 368 ugucauugau ugucgcuau 19 <210> SEQ ID NO 369 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA <400> SEQUENCE: 369 uugauugucg cuauccaua 19 <210> SEQ ID NO 370 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA <400> SEQUENCE: 370 uugucgcuau ccauaugag 19 <210> SEQ ID NO 371 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA <400> SEQUENCE: 371 uccagggagc cuuaaacuu 19 <210> SEQ ID NO 372 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA <400> SEQUENCE: 372 gggagccuua aacuuauau 19 <210> SEQ ID NO 373 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA <400> SEQUENCE: 373 gucaggaaga acuguuuaa 19 <210> SEQ ID NO 374 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA <400> SEQUENCE: 374 agaagcccau cgucccuuu 19 <210> SEQ ID NO 375 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA <400> SEQUENCE: 375 gaagcccauc gucccuuug 19 <210> SEQ ID NO 376 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA <400> SEQUENCE: 376 agcccaucgu cccuuugga 19 <210> SEQ ID NO 377 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA <400> SEQUENCE: 377 cacccagaag agaauaauc 19 <210> SEQ ID NO 378 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA <400> SEQUENCE: 378 uuguacuacc cagagcuau 19 <210> SEQ ID NO 379 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA <400> SEQUENCE: 379 cuacccagag cuauauauc 19 <210> SEQ ID NO 380 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA <400> SEQUENCE: 380 cccagagcua uauauccuu 19 <210> SEQ ID NO 381 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA <400> SEQUENCE: 381 uauauggaac ugugugaac 19 <210> SEQ ID NO 382 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA <400> SEQUENCE: 382 uauggaacug ugugaacca 19 <210> SEQ ID NO 383 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA <400> SEQUENCE: 383 cagagcuacu gcccuaugc 19 <210> SEQ ID NO 384 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA <400> SEQUENCE: 384 gagcuacugc ccuaugcau 19 <210> SEQ ID NO 385 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA <400> SEQUENCE: 385 gcuacugccc uaugcauca 19 <210> SEQ ID NO 386 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA <400> SEQUENCE: 386 gaugaagagc cuauugaag 19 <210> SEQ ID NO 387 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA <400> SEQUENCE: 387 agaugaacag acuccaauu 19 <210> SEQ ID NO 388 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA <400> SEQUENCE: 388 gaugaacaga cuccaauuc 19 <210> SEQ ID NO 389 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA <400> SEQUENCE: 389 ucacccauca ucauccaau 19 <210> SEQ ID NO 390 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA <400> SEQUENCE: 390 gagcuuacaa ccugccuua 19 <210> SEQ ID NO 391 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA <400> SEQUENCE: 391 cacugcuaug gaggacuug 19 <210> SEQ ID NO 392 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA <400> SEQUENCE: 392 ucaccagagc aagccauag 19 <210> SEQ ID NO 393 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA <400> SEQUENCE: 393 ccagagcaag ccauagaca 19 <210> SEQ ID NO 394 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA <400> SEQUENCE: 394 cagccugcga gaccuaaga 19 <210> SEQ ID NO 395 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA <400> SEQUENCE: 395 guuucgggac aaauuagcu 19 <210> SEQ ID NO 396 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA <400> SEQUENCE: 396 aauuagcugc acaucuauc 19 <210> SEQ ID NO 397 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA <400> SEQUENCE: 397 auuagcugca caucuauca 19 <210> SEQ ID NO 398 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA <400> SEQUENCE: 398 uuagcugcac aucuaucau 19 <210> SEQ ID NO 399 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA <400> SEQUENCE: 399 gagacgcgga acaauugag 19 <210> SEQ ID NO 400 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA <400> SEQUENCE: 400 agaacaaggu gacacauau 19 <210> SEQ ID NO 401 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA <400> SEQUENCE: 401 gaacaaggug acacauauu 19 <210> SEQ ID NO 402 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA <400> SEQUENCE: 402 gcagcggauu caccaucuc 19 <210> SEQ ID NO 403 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA <400> SEQUENCE: 403 gcggauucac caucucaaa 19 <210> SEQ ID NO 404 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA <400> SEQUENCE: 404 cacuggugau cgcauacau 19 <210> SEQ ID NO 405 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA <400> SEQUENCE: 405 guaucggcag uggcugaag 19 <210> SEQ ID NO 406 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA <400> SEQUENCE: 406 gauccgccga cgacugcaa 19 <210> SEQ ID NO 407 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA <400> SEQUENCE: 407 guuucgggag gaguucaac 19 <210> SEQ ID NO 408 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA <400> SEQUENCE: 408 augaccauuc uagggugau 19 <210> SEQ ID NO 409 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA <400> SEQUENCE: 409 ccauucuagg gugauucug 19 <210> SEQ ID NO 410 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA <400> SEQUENCE: 410 cauagauggu uacaaagag 19 <210> SEQ ID NO 411 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA <400> SEQUENCE: 411 aacaggaaac gguuaacga 19 <210> SEQ ID NO 412 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA <400> SEQUENCE: 412 ggaaacgguu aacgacuuc 19 <210> SEQ ID NO 413 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA <400> SEQUENCE: 413 ccaucgucau guuaacaaa 19 <210> SEQ ID NO 414 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA <400> SEQUENCE: 414 cuacaccauc cggaaguuc 19 <210> SEQ ID NO 415 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA <400> SEQUENCE: 415 uccggaaguu cugcauaca 19 <210> SEQ ID NO 416 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA <400> SEQUENCE: 416 gaaaguaaag acgcucaac 19 <210> SEQ ID NO 417 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA <400> SEQUENCE: 417 gcgcccucag augguucaa 19 <210> SEQ ID NO 418 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA <400> SEQUENCE: 418 cggauaugca guacacguu 19 <210> SEQ ID NO 419 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA <400> SEQUENCE: 419 ccacccacuu cgacaagau 19 <210> SEQ ID NO 420 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA <400> SEQUENCE: 420 caaauguccg gaucaugaa 19 <210> SEQ ID NO 421 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA <400> SEQUENCE: 421 caugaggacg ggcaacuug 19 <210> SEQ ID NO 422 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA <400> SEQUENCE: 422 ugacuucaac cgagugauc 19 <210> SEQ ID NO 423 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA <400> SEQUENCE: 423 accgagugau ccuuuccau 19 <210> SEQ ID NO 424 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA <400> SEQUENCE: 424 agaauacaca gacuacauc 19 <210> SEQ ID NO 425 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA <400> SEQUENCE: 425 gacuacauca acgcauccu 19 <210> SEQ ID NO 426 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA <400> SEQUENCE: 426 ucaacgcauc cuucauaga 19 <210> SEQ ID NO 427 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA <400> SEQUENCE: 427 cacacgguug aggacuucu 19 <210> SEQ ID NO 428 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA <400> SEQUENCE: 428 aaucccacac uaucgugau 19 <210> SEQ ID NO 429 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA <400> SEQUENCE: 429 aucccacacu aucgugaug 19 <210> SEQ ID NO 430 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA <400> SEQUENCE: 430 accgagggcu caguuacuc 19 <210> SEQ ID NO 431 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA <400> SEQUENCE: 431 ccgagggcuc aguuacuca 19 <210> SEQ ID NO 432 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA <400> SEQUENCE: 432 cucauggaga aauaacgau 19 <210> SEQ ID NO 433 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA <400> SEQUENCE: 433 uggagaaaua acgauugag 19 <210> SEQ ID NO 434 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA <400> SEQUENCE: 434 gccaucagua uacgagacu 19 <210> SEQ ID NO 435 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA <400> SEQUENCE: 435 ucaguauacg agacuuucu 19 <210> SEQ ID NO 436 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA <400> SEQUENCE: 436 gggcaaaggc augauugac 19 <210> SEQ ID NO 437 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA <400> SEQUENCE: 437 gcugggcgaa cagguacau 19 <210> SEQ ID NO 438 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA <400> SEQUENCE: 438 cuucagagac cacauaugg 19 <210> SEQ ID NO 439 <211> LENGTH: 21 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - cdc14a.2 <400> SEQUENCE: 439 caucugugag aacaccgaat t 21 <210> SEQ ID NO 440 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - cdc14a.2 <400> SEQUENCE: 440 caucugugag aacaccgaa 19 <210> SEQ ID NO 441 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - cdc14a.2 <400> SEQUENCE: 441 uucgguguuc ucacagaug 19 <210> SEQ ID NO 442 <211> LENGTH: 21 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - cdc14a.2 <220> FEATURE: <221> NAME/KEY: misc_feature <222> LOCATION: 20, 21 <223> OTHER INFORMATION: n = A,T,C,G or U <400> SEQUENCE: 442 caucugugag aacaccgaan n 21 <210> SEQ ID NO 443 <211> LENGTH: 21 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - cdc14a.2 <220> FEATURE: <221> NAME/KEY: misc_feature <222> LOCATION: 1, 2 <223> OTHER INFORMATION: n = A,T,C,G or U <400> SEQUENCE: 443 nnuucggugu ucucacagau g 21 <210> SEQ ID NO 444 <211> LENGTH: 21 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - cdc14a.3 <400> SEQUENCE: 444 cuuggcaaug guguacagat t 21 <210> SEQ ID NO 445 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - cdc14a.3 <400> SEQUENCE: 445 cuuggcaaug guguacaga 19 <210> SEQ ID NO 446 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - cdc14a.3 <400> SEQUENCE: 446 ucuguacacc auugccaag 19 <210> SEQ ID NO 447 <211> LENGTH: 21 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - cdc14a.3 <220> FEATURE: <221> NAME/KEY: misc_feature <222> LOCATION: 20, 21 <223> OTHER INFORMATION: n = A,T,C,G or U <400> SEQUENCE: 447 cuuggcaaug guguacagan n 21 <210> SEQ ID NO 448 <211> LENGTH: 21 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - cdc14a.3 <220> FEATURE: <221> NAME/KEY: misc_feature <222> LOCATION: 1, 2 <223> OTHER INFORMATION: n = A,T,C,G or U <400> SEQUENCE: 448 nnucuguaca ccauugccaa g 21 <210> SEQ ID NO 449 <211> LENGTH: 21 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - cdc14a.5 <400> SEQUENCE: 449 gcacaguaaa uacccacuat t 21 <210> SEQ ID NO 450 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - cdc14a.5 <400> SEQUENCE: 450 gcacaguaaa uacccacua 19 <210> SEQ ID NO 451 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - cdc14a.5 <400> SEQUENCE: 451 uaguggguau uuacugugc 19 <210> SEQ ID NO 452 <211> LENGTH: 21 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - cdc14a.5 <220> FEATURE: <221> NAME/KEY: misc_feature <222> LOCATION: 20, 21 <223> OTHER INFORMATION: n = A,T,C,G or U <400> SEQUENCE: 452 gcacaguaaa uacccacuan n 21 <210> SEQ ID NO 453 <211> LENGTH: 21 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - cdc14a.5 <220> FEATURE: <221> NAME/KEY: misc_feature <222> LOCATION: 1, 2 <223> OTHER INFORMATION: n = A,T,C,G or U <400> SEQUENCE: 453 nnuagugggu auuuacugug c 21 <210> SEQ ID NO 454 <211> LENGTH: 21 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - cdc14b.3 <400> SEQUENCE: 454 caagcaaaug cugccuucct t 21 <210> SEQ ID NO 455 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - cdc14b.3 <400> SEQUENCE: 455 caagcaaaug cugccuucc 19 <210> SEQ ID NO 456 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - cdc14b.3 <400> SEQUENCE: 456 ggaaggcagc auuugcuug 19 <210> SEQ ID NO 457 <211> LENGTH: 21 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - cdc14b.3 <220> FEATURE: <221> NAME/KEY: misc_feature <222> LOCATION: 20, 21 <223> OTHER INFORMATION: n = A,T,C,G or U <400> SEQUENCE: 457 caagcaaaug cugccuuccn n 21 <210> SEQ ID NO 458 <211> LENGTH: 21 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - cdc14b.3 <220> FEATURE: <221> NAME/KEY: misc_feature <222> LOCATION: 1, 2 <223> OTHER INFORMATION: n = A,T,C,G or U <400> SEQUENCE: 458 nnggaaggca gcauuugcuu g 21 <210> SEQ ID NO 459 <211> LENGTH: 21 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - cdc14b.4 <400> SEQUENCE: 459 gagccagacu ugaaaguggt t 21 <210> SEQ ID NO 460 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - cdc14b.4 <400> SEQUENCE: 460 gagccagacu ugaaagugg 19 <210> SEQ ID NO 461 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - cdc14b.4 <400> SEQUENCE: 461 ccacuuucaa gucuggcuc 19 <210> SEQ ID NO 462 <211> LENGTH: 21 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - cdc14b.4 <220> FEATURE: <221> NAME/KEY: misc_feature <222> LOCATION: 20, 21 <223> OTHER INFORMATION: n = A,T,C,G or U <400> SEQUENCE: 462 gagccagacu ugaaaguggn n 21 <210> SEQ ID NO 463 <211> LENGTH: 21 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - cdc14b.4 <220> FEATURE: <221> NAME/KEY: misc_feature <222> LOCATION: 1, 2 <223> OTHER INFORMATION: n = A,T,C,G or U <400> SEQUENCE: 463 nnccacuuuc aagucuggcu c 21 <210> SEQ ID NO 464 <211> LENGTH: 21 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - 25 A.2 <400> SEQUENCE: 464 gaggagccau ucugauucut t 21 <210> SEQ ID NO 465 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - 25 A.2 <400> SEQUENCE: 465 gaggagccau ucugauucu 19 <210> SEQ ID NO 466 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - 25 A.2 <400> SEQUENCE: 466 agaaucagaa uggcuccuc 19 <210> SEQ ID NO 467 <211> LENGTH: 21 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - 25 A.2 <220> FEATURE: <221> NAME/KEY: misc_feature <222> LOCATION: 20, 21 <223> OTHER INFORMATION: n = A,T,C,G or U <400> SEQUENCE: 467 gaggagccau ucugauucun n 21 <210> SEQ ID NO 468 <211> LENGTH: 21 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - 25 A.2 <220> FEATURE: <221> NAME/KEY: misc_feature <222> LOCATION: 1, 2 <223> OTHER INFORMATION: n = A,T,C,G or U <400> SEQUENCE: 468 nnagaaucag aauggcuccu c 21 <210> SEQ ID NO 469 <211> LENGTH: 21 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - cdc25B.2 <400> SEQUENCE: 469 aggcggcuac aaggaguuct t 21 <210> SEQ ID NO 470 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - cdc25B.2 <400> SEQUENCE: 470 aggcggcuac aaggaguuc 19 <210> SEQ ID NO 471 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - cdc25B.2 <400> SEQUENCE: 471 gaacuccuug uagccgccu 19 <210> SEQ ID NO 472 <211> LENGTH: 21 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - cdc25B.2 <220> FEATURE: <221> NAME/KEY: misc_feature <222> LOCATION: 20, 21 <223> OTHER INFORMATION: n = A,T,C,G or U <400> SEQUENCE: 472 aggcggcuac aaggaguucn n 21 <210> SEQ ID NO 473 <211> LENGTH: 21 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - cdc25B.2 <220> FEATURE: <221> NAME/KEY: misc_feature <222> LOCATION: 1, 2 <223> OTHER INFORMATION: n = A,T,C,G or U <400> SEQUENCE: 473 nngaacuccu uguagccgcc u 21 <210> SEQ ID NO 474 <211> LENGTH: 21 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - cdc25B.4 <400> SEQUENCE: 474 gaugccaugg aagcccacat t 21 <210> SEQ ID NO 475 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - cdc25B.4 <400> SEQUENCE: 475 gaugccaugg aagcccaca 19 <210> SEQ ID NO 476 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - cdc25B.4 <400> SEQUENCE: 476 ugugggcuuc cauggcauc 19 <210> SEQ ID NO 477 <211> LENGTH: 21 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - cdc25B.4 <220> FEATURE: <221> NAME/KEY: misc_feature <222> LOCATION: 20, 21 <223> OTHER INFORMATION: n = A,T,C,G or U <400> SEQUENCE: 477 gaugccaugg aagcccacan n 21 <210> SEQ ID NO 478 <211> LENGTH: 21 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - cdc25B.4 <220> FEATURE: <221> NAME/KEY: misc_feature <222> LOCATION: 1, 2 <223> OTHER INFORMATION: n = A,T,C,G or U <400> SEQUENCE: 478 nnugugggcu uccauggcau c 21 <210> SEQ ID NO 479 <211> LENGTH: 21 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - cdc25C.1 <400> SEQUENCE: 479 cugccacuca gcuuaccact t 21 <210> SEQ ID NO 480 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - cdc25C.1 <400> SEQUENCE: 480 cugccacuca gcuuaccac 19 <210> SEQ ID NO 481 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - cdc25C.1 <400> SEQUENCE: 481 gugguaagcu gaguggcag 19 <210> SEQ ID NO 482 <211> LENGTH: 21 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - cdc25C.1 <220> FEATURE: <221> NAME/KEY: misc_feature <222> LOCATION: 20, 21 <223> OTHER INFORMATION: n = A,T,C,G or U <400> SEQUENCE: 482 cugccacuca gcuuaccacn n 21 <210> SEQ ID NO 483 <211> LENGTH: 21 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - cdc25C.1 <220> FEATURE: <221> NAME/KEY: misc_feature <222> LOCATION: 1, 2 <223> OTHER INFORMATION: n = A,T,C,G or U <400> SEQUENCE: 483 nngugguaag cugaguggca g 21 <210> SEQ ID NO 484 <211> LENGTH: 21 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - cdc25C.3 <400> SEQUENCE: 484 cccagaaaca guggcugcct t 21 <210> SEQ ID NO 485 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - cdc25C.3 <400> SEQUENCE: 485 cccagaaaca guggcugcc 19 <210> SEQ ID NO 486 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - cdc25C.3 <400> SEQUENCE: 486 ggcagccacu guuucuggg 19 <210> SEQ ID NO 487 <211> LENGTH: 21 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - cdc25C.3 <220> FEATURE: <221> NAME/KEY: misc_feature <222> LOCATION: 20, 21 <223> OTHER INFORMATION: n = A,T,C,G or U <400> SEQUENCE: 487 cccagaaaca guggcugccn n 21 <210> SEQ ID NO 488 <211> LENGTH: 21 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - cdc25C.3 <220> FEATURE: <221> NAME/KEY: misc_feature <222> LOCATION: 1, 2 <223> OTHER INFORMATION: n = A,T,C,G or U <400> SEQUENCE: 488 nnggcagcca cuguuucugg g 21 <210> SEQ ID NO 489 <211> LENGTH: 21 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - cdc25C.4 <400> SEQUENCE: 489 aggcggcuac agagacuuct t 21 <210> SEQ ID NO 490 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - cdc25C.4 <400> SEQUENCE: 490 aggcggcuac agagacuuc 19 <210> SEQ ID NO 491 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - cdc25C.4 <400> SEQUENCE: 491 gaagucucug uagccgccu 19 <210> SEQ ID NO 492 <211> LENGTH: 21 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - cdc25C.4 <220> FEATURE: <221> NAME/KEY: misc_feature <222> LOCATION: 20, 21 <223> OTHER INFORMATION: n = A,T,C,G or U <400> SEQUENCE: 492 aggcggcuac agagacuucn n 21 <210> SEQ ID NO 493 <211> LENGTH: 21 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - cdc25C.4 <220> FEATURE: <221> NAME/KEY: misc_feature <222> LOCATION: 1, 2 <223> OTHER INFORMATION: n = A,T,C,G or U <400> SEQUENCE: 493 nngaagucuc uguagccgcc u 21 <210> SEQ ID NO 494 <211> LENGTH: 36 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Oligonucleotide primer mPTP1B-sense <400> SEQUENCE: 494 gggggggatc catggagatg gagaaggagt tcgagg 36 <210> SEQ ID NO 495 <211> LENGTH: 35 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Oligonucleotide primer mPTP1B anti-sense <400> SEQUENCE: 495 gggggaattc tcagtgaaaa cacacccggt agcac 35 <210> SEQ ID NO 496 <211> LENGTH: 21 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - mPTP1B1.1 <400> SEQUENCE: 496 gaagcccaga ggagcuauat t 21 <210> SEQ ID NO 497 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - mPTP1B1.1 <400> SEQUENCE: 497 gaagcccaga ggagcuaua 19 <210> SEQ ID NO 498 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - mPTP1B1.1 <400> SEQUENCE: 498 uauagcuccu cugggcuuc 19 <210> SEQ ID NO 499 <211> LENGTH: 21 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - mPTP1B1.1 <220> FEATURE: <221> NAME/KEY: misc_feature <222> LOCATION: 20, 21 <223> OTHER INFORMATION: n = A,T,C,G or U <400> SEQUENCE: 499 gaagcccaga ggagcuauan n 21 <210> SEQ ID NO 500 <211> LENGTH: 21 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - mPTP1B1.1 <220> FEATURE: <221> NAME/KEY: misc_feature <222> LOCATION: 1, 2 <223> OTHER INFORMATION: n = A,T,C,G or U <400> SEQUENCE: 500 nnuauagcuc cucugggcuu c 21 <210> SEQ ID NO 501 <211> LENGTH: 21 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - mPTP1B1.2 <400> SEQUENCE: 501 cuacaccaca uggccugact t 21 <210> SEQ ID NO 502 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - mPTP1B1.2 <400> SEQUENCE: 502 cuacaccaca uggccugac 19 <210> SEQ ID NO 503 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - mPTP1B1.2 <400> SEQUENCE: 503 gucaggccau gugguguag 19 <210> SEQ ID NO 504 <211> LENGTH: 21 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - mPTP1B1.2 <220> FEATURE: <221> NAME/KEY: misc_feature <222> LOCATION: 20, 21 <223> OTHER INFORMATION: n = A,T,C,G or U <400> SEQUENCE: 504 cuacaccaca uggccugacn n 21 <210> SEQ ID NO 505 <211> LENGTH: 21 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - mPTP1B1.2 <220> FEATURE: <221> NAME/KEY: misc_feature <222> LOCATION: 1, 2 <223> OTHER INFORMATION: n = A,T,C,G or U <400> SEQUENCE: 505 nngucaggcc auguggugua g 21 <210> SEQ ID NO 506 <211> LENGTH: 21 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - mPTP1B1.3 <400> SEQUENCE: 506 gacugccgac cagcugcgct t 21 <210> SEQ ID NO 507 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - mPTP1B1.3 <400> SEQUENCE: 507 gacugccgac cagcugcgc 19 <210> SEQ ID NO 508 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - mPTP1B1.3 <400> SEQUENCE: 508 gcgcagcugg ucggcaguc 19 <210> SEQ ID NO 509 <211> LENGTH: 21 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - mPTP1B1.3 <220> FEATURE: <221> NAME/KEY: misc_feature <222> LOCATION: 20, 21 <223> OTHER INFORMATION: n = A,T,C,G or U <400> SEQUENCE: 509 gacugccgac cagcugcgcn n 21 <210> SEQ ID NO 510 <211> LENGTH: 21 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - mPTP1B1.3 <220> FEATURE: <221> NAME/KEY: misc_feature <222> LOCATION: 1, 2 <223> OTHER INFORMATION: n = A,T,C,G or U <400> SEQUENCE: 510 nngcgcagcu ggucggcagu c 21 <210> SEQ ID NO 511 <211> LENGTH: 21 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - mPTP1B1.4 <400> SEQUENCE: 511 gguaccgaga ugucagccct t 21 <210> SEQ ID NO 512 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - mPTP1B1.4 <400> SEQUENCE: 512 gguaccgaga ugucagccc 19 <210> SEQ ID NO 513 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - mPTP1B1.4 <400> SEQUENCE: 513 gggcugacau cucgguacc 19 <210> SEQ ID NO 514 <211> LENGTH: 21 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - mPTP1B1.4 <220> FEATURE: <221> NAME/KEY: misc_feature <222> LOCATION: 20, 21 <223> OTHER INFORMATION: n = A,T,C,G or U <400> SEQUENCE: 514 gguaccgaga ugucagcccn n 21 <210> SEQ ID NO 515 <211> LENGTH: 21 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - mPTP1B1.4 <220> FEATURE: <221> NAME/KEY: misc_feature <222> LOCATION: 1, 2 <223> OTHER INFORMATION: n = A,T,C,G or U <400> SEQUENCE: 515 nngggcugac aucucgguac c 21 <210> SEQ ID NO 516 <211> LENGTH: 21 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - mPTP1B1.5 <400> SEQUENCE: 516 ugacuauauc aaugccagct t 21 <210> SEQ ID NO 517 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - mPTP1B1.5 <400> SEQUENCE: 517 ugacuauauc aaugccagc 19 <210> SEQ ID NO 518 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - mPTP1B1.5 <400> SEQUENCE: 518 gcuggcauug auauaguca 19 <210> SEQ ID NO 519 <211> LENGTH: 21 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - mPTP1B1.5 <220> FEATURE: <221> NAME/KEY: misc_feature <222> LOCATION: 20, 21 <223> OTHER INFORMATION: n = A,T,C,G or U <400> SEQUENCE: 519 ugacuauauc aaugccagcn n 21 <210> SEQ ID NO 520 <211> LENGTH: 21 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - mPTP1B1.5 <220> FEATURE: <221> NAME/KEY: misc_feature <222> LOCATION: 1, 2 <223> OTHER INFORMATION: n = A,T,C,G or U <400> SEQUENCE: 520 nngcuggcau ugauauaguc a 21 <210> SEQ ID NO 521 <211> LENGTH: 21 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - mPTP1B1.6 <400> SEQUENCE: 521 agaagaaaag gagaugguct t 21 <210> SEQ ID NO 522 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - mPTP1B1.6 <400> SEQUENCE: 522 agaagaaaag gagaugguc 19 <210> SEQ ID NO 523 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - mPTP1B1.6 <400> SEQUENCE: 523 gaccaucucc uuuucuucu 19 <210> SEQ ID NO 524 <211> LENGTH: 21 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - mPTP1B1.6 <220> FEATURE: <221> NAME/KEY: misc_feature <222> LOCATION: 20, 21 <223> OTHER INFORMATION: n = A,T,C,G or U <400> SEQUENCE: 524 agaagaaaag gagauggucn n 21 <210> SEQ ID NO 525 <211> LENGTH: 21 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - mPTP1B1.6 <220> FEATURE: <221> NAME/KEY: misc_feature <222> LOCATION: 1, 2 <223> OTHER INFORMATION: n = A,T,C,G or U <400> SEQUENCE: 525 nngaccaucu ccuuuucuuc u 21 <210> SEQ ID NO 526 <211> LENGTH: 21 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - mPTP1B1.7 <400> SEQUENCE: 526 cgggaagugc aaggagcuct t 21 <210> SEQ ID NO 527 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - mPTP1B1.7 <400> SEQUENCE: 527 cgggaagugc aaggagcuc 19 <210> SEQ ID NO 528 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - mPTP1B1.7 <400> SEQUENCE: 528 gagcuccuug cacuucccg 19 <210> SEQ ID NO 529 <211> LENGTH: 21 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - mPTP1B1.7 <220> FEATURE: <221> NAME/KEY: misc_feature <222> LOCATION: 20, 21 <223> OTHER INFORMATION: n = A,T,C,G or U <400> SEQUENCE: 529 cgggaagugc aaggagcucn n 21 <210> SEQ ID NO 530 <211> LENGTH: 21 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - mPTP1B1.7 <220> FEATURE: <221> NAME/KEY: misc_feature <222> LOCATION: 1, 2 <223> OTHER INFORMATION: n = A,T,C,G or U <400> SEQUENCE: 530 nngagcuccu ugcacuuccc g 21 <210> SEQ ID NO 531 <211> LENGTH: 21 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - mPTP1B1.8 <400> SEQUENCE: 531 ggaucagugg aaggagcuct c 21 <210> SEQ ID NO 532 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - mPTP1B1.8 <400> SEQUENCE: 532 ggaucagugg aaggagcuc 19 <210> SEQ ID NO 533 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - mPTP1B1.8 <400> SEQUENCE: 533 gagcuccuuc cacugaucc 19 <210> SEQ ID NO 534 <211> LENGTH: 21 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - mPTP1B1.8 <220> FEATURE: <221> NAME/KEY: misc_feature <222> LOCATION: 20, 21 <223> OTHER INFORMATION: n = A,T,C,G or U <400> SEQUENCE: 534 ggaucagugg aaggagcucn n 21 <210> SEQ ID NO 535 <211> LENGTH: 21 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - mPTP1B1.8 <220> FEATURE: <221> NAME/KEY: misc_feature <222> LOCATION: 1, 2 <223> OTHER INFORMATION: n = A,T,C,G or U <400> SEQUENCE: 535 nngagcuccu uccacugauc c 21 <210> SEQ ID NO 536 <211> LENGTH: 21 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - rPTP1B1.1 <400> SEQUENCE: 536 agaagaaaaa gagaugguct t 21 <210> SEQ ID NO 537 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - rPTP1B1.1 <400> SEQUENCE: 537 agaagaaaaa gagaugguc 19 <210> SEQ ID NO 538 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - rPTP1B1.1 <400> SEQUENCE: 538 gaccaucucu uuuucuucu 19 <210> SEQ ID NO 539 <211> LENGTH: 21 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - rPTP1B1.1 <220> FEATURE: <221> NAME/KEY: misc_feature <222> LOCATION: 20, 21 <223> OTHER INFORMATION: n = A,T,C,G or U <400> SEQUENCE: 539 agaagaaaaa gagauggucn n 21 <210> SEQ ID NO 540 <211> LENGTH: 21 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - rPTP1B1.1 <220> FEATURE: <221> NAME/KEY: misc_feature <222> LOCATION: 1, 2 <223> OTHER INFORMATION: n = A,T,C,G or U <400> SEQUENCE: 540 nngaccaucu cuuuuucuuc u 21 <210> SEQ ID NO 541 <211> LENGTH: 21 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - rPTP1B1.2 <400> SEQUENCE: 541 cggauggugg guggagguct t 21 <210> SEQ ID NO 542 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - rPTP1B1.2 <400> SEQUENCE: 542 cggauggugg guggagguc 19 <210> SEQ ID NO 543 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - rPTP1B1.2 <400> SEQUENCE: 543 gaccuccacc caccauccg 19 <210> SEQ ID NO 544 <211> LENGTH: 21 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - rPTP1B1.2 <220> FEATURE: <221> NAME/KEY: misc_feature <222> LOCATION: 20, 21 <223> OTHER INFORMATION: n = A,T,C,G or U <400> SEQUENCE: 544 cggauggugg guggaggucn n 21 <210> SEQ ID NO 545 <211> LENGTH: 21 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - rPTP1B1.2 <220> FEATURE: <221> NAME/KEY: misc_feature <222> LOCATION: 1, 2 <223> OTHER INFORMATION: n = A,T,C,G or U <400> SEQUENCE: 545 nngaccucca cccaccaucc g 21 <210> SEQ ID NO 546 <211> LENGTH: 21 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - rPTP1B1.3 <400> SEQUENCE: 546 uggcaagugc aaggagcuct t 21 <210> SEQ ID NO 547 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - rPTP1B1.3 <400> SEQUENCE: 547 uggcaagugc aaggagcuc 19 <210> SEQ ID NO 548 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - rPTP1B1.3 <400> SEQUENCE: 548 gagcuccuug cacuugcca 19 <210> SEQ ID NO 549 <211> LENGTH: 21 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - rPTP1B1.3 <220> FEATURE: <221> NAME/KEY: misc_feature <222> LOCATION: 20, 21 <223> OTHER INFORMATION: n = A,T,C,G or U <400> SEQUENCE: 549 uggcaagugc aaggagcucn n 21 <210> SEQ ID NO 550 <211> LENGTH: 21 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - rPTP1B1.3 <220> FEATURE: <221> NAME/KEY: misc_feature <222> LOCATION: 1, 2 <223> OTHER INFORMATION: n = A,T,C,G or U <400> SEQUENCE: 550 nngagcuccu ugcacuugcc a 21 <210> SEQ ID NO 551 <211> LENGTH: 21 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - rPTP1B1.4 <400> SEQUENCE: 551 cuacaccacc uggccugact t 21 <210> SEQ ID NO 552 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - rPTP1B1.4 <400> SEQUENCE: 552 cuacaccacc uggccugac 19 <210> SEQ ID NO 553 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - rPTP1B1.4 <400> SEQUENCE: 553 gucaggccag gugguguag 19 <210> SEQ ID NO 554 <211> LENGTH: 21 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - rPTP1B1.4 <220> FEATURE: <221> NAME/KEY: misc_feature <222> LOCATION: 20, 21 <223> OTHER INFORMATION: n = A,T,C,G or U <400> SEQUENCE: 554 cuacaccacc uggccugacn n 21 <210> SEQ ID NO 555 <211> LENGTH: 21 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - rPTP1B1.4 <220> FEATURE: <221> NAME/KEY: misc_feature <222> LOCATION: 1, 2 <223> OTHER INFORMATION: n = A,T,C,G or U <400> SEQUENCE: 555 nngucaggcc agguggugua g 21 <210> SEQ ID NO 556 <211> LENGTH: 21 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - hPTP1B1.1 <400> SEQUENCE: 556 cuauaccaca uggccugact t 21 <210> SEQ ID NO 557 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - hPTP1B1.1 <400> SEQUENCE: 557 cuauaccaca uggccugac 19 <210> SEQ ID NO 558 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - hPTP1B1.1 <400> SEQUENCE: 558 gucaggccau gugguauag 19 <210> SEQ ID NO 559 <211> LENGTH: 21 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - hPTP1B1.1 <220> FEATURE: <221> NAME/KEY: misc_feature <222> LOCATION: 20, 21 <223> OTHER INFORMATION: n = A,T,C,G or U <400> SEQUENCE: 559 cuauaccaca uggccugacn n 21 <210> SEQ ID NO 560 <211> LENGTH: 21 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - hPTP1B1.1 <220> FEATURE: <221> NAME/KEY: misc_feature <222> LOCATION: 1, 2 <223> OTHER INFORMATION: n = A,T,C,G or U <400> SEQUENCE: 560 nngucaggcc augugguaua g 21 <210> SEQ ID NO 561 <211> LENGTH: 21 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - hPTP1B1.2 <400> SEQUENCE: 561 gcccaaagga guuacauuct t 21 <210> SEQ ID NO 562 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - hPTP1B1.2 <400> SEQUENCE: 562 gcccaaagga guuacauuc 19 <210> SEQ ID NO 563 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - hPTP1B1.2 <400> SEQUENCE: 563 gaauguaacu ccuuugggc 19 <210> SEQ ID NO 564 <211> LENGTH: 21 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - hPTP1B1.2 <220> FEATURE: <221> NAME/KEY: misc_feature <222> LOCATION: 20, 21 <223> OTHER INFORMATION: n = A,T,C,G or U <400> SEQUENCE: 564 gcccaaagga guuacauucn n 21 <210> SEQ ID NO 565 <211> LENGTH: 21 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - hPTP1B1.2 <220> FEATURE: <221> NAME/KEY: misc_feature <222> LOCATION: 1, 2 <223> OTHER INFORMATION: n = A,T,C,G or U <400> SEQUENCE: 565 nngaauguaa cuccuuuggg c 21 <210> SEQ ID NO 566 <211> LENGTH: 21 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - hPTP1B1.3 <400> SEQUENCE: 566 ggaagaaaaa ggaagcccct t 21 <210> SEQ ID NO 567 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - hPTP1B1.3 <400> SEQUENCE: 567 ggaagaaaaa ggaagcccc 19 <210> SEQ ID NO 568 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - hPTP1B1.3 <400> SEQUENCE: 568 ggggcuuccu uuuucuucc 19 <210> SEQ ID NO 569 <211> LENGTH: 21 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - hPTP1B1.3 <220> FEATURE: <221> NAME/KEY: misc_feature <222> LOCATION: 20, 21 <223> OTHER INFORMATION: n = A,T,C,G or U <400> SEQUENCE: 569 ggaagaaaaa ggaagccccn n 21 <210> SEQ ID NO 570 <211> LENGTH: 21 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - hPTP1B1.3 <220> FEATURE: <221> NAME/KEY: misc_feature <222> LOCATION: 1, 2 <223> OTHER INFORMATION: n = A,T,C,G or U <400> SEQUENCE: 570 nnggggcuuc cuuuuucuuc c 21 <210> SEQ ID NO 571 <211> LENGTH: 21 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - hPTP1B1.4 <400> SEQUENCE: 571 caaugggaaa ugcagggagt t 21 <210> SEQ ID NO 572 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - hPTP1B1.4 <400> SEQUENCE: 572 caaugggaaa ugcagggag 19 <210> SEQ ID NO 573 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - hPTP1B1.4 <400> SEQUENCE: 573 cucccugcau uucccauug 19 <210> SEQ ID NO 574 <211> LENGTH: 21 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - hPTP1B1.4 <220> FEATURE: <221> NAME/KEY: misc_feature <222> LOCATION: 20, 21 <223> OTHER INFORMATION: n = A,T,C,G or U <400> SEQUENCE: 574 caaugggaaa ugcagggagn n 21 <210> SEQ ID NO 575 <211> LENGTH: 21 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - hPTP1B1.4 <220> FEATURE: <221> NAME/KEY: misc_feature <222> LOCATION: 1, 2 <223> OTHER INFORMATION: n = A,T,C,G or U <400> SEQUENCE: 575 nncucccugc auuucccauu g 21 <210> SEQ ID NO 576 <211> LENGTH: 21 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - hPTP1B1.5 <400> SEQUENCE: 576 ggaucagugg aaggagcuut c 21 <210> SEQ ID NO 577 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - hPTP1B1.5 <400> SEQUENCE: 577 ggaucagugg aaggagcuu 19 <210> SEQ ID NO 578 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - hPTP1B1.5 <400> SEQUENCE: 578 aagcuccuuc cacugaucc 19 <210> SEQ ID NO 579 <211> LENGTH: 21 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - hPTP1B1.5 <220> FEATURE: <221> NAME/KEY: misc_feature <222> LOCATION: 20, 21 <223> OTHER INFORMATION: n = A,T,C,G or U <400> SEQUENCE: 579 ggaucagugg aaggagcuun n 21 <210> SEQ ID NO 580 <211> LENGTH: 21 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - hPTP1B1.5 <220> FEATURE: <221> NAME/KEY: misc_feature <222> LOCATION: 1, 2 <223> OTHER INFORMATION: n = A,T,C,G or U <400> SEQUENCE: 580 nnaagcuccu uccacugauc c 21 <210> SEQ ID NO 581 <211> LENGTH: 21 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - mTCPTP1.1 <400> SEQUENCE: 581 guugucaugc uaaaccgaac t 21 <210> SEQ ID NO 582 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - mTCPTP1.1 <400> SEQUENCE: 582 guugucaugc uaaaccgaa 19 <210> SEQ ID NO 583 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - mTCPTP1.1 <400> SEQUENCE: 583 uucgguuuag caugacaac 19 <210> SEQ ID NO 584 <211> LENGTH: 21 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - mTCPTP1.1 <220> FEATURE: <221> NAME/KEY: misc_feature <222> LOCATION: 20, 21 <223> OTHER INFORMATION: n = A,T,C,G or U <400> SEQUENCE: 584 guugucaugc uaaaccgaan n 21 <210> SEQ ID NO 585 <211> LENGTH: 21 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - mTCPTP1.1 <220> FEATURE: <221> NAME/KEY: misc_feature <222> LOCATION: 1, 2 <223> OTHER INFORMATION: n = A,T,C,G or U <400> SEQUENCE: 585 nnuucgguuu agcaugacaa c 21 <210> SEQ ID NO 586 <211> LENGTH: 21 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - mTCPTP1.2 <400> SEQUENCE: 586 cagaacagag ugaugguuga g 21 <210> SEQ ID NO 587 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - mTCPTP1.2 <400> SEQUENCE: 587 cagaacagag ugaugguug 19 <210> SEQ ID NO 588 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - mTCPTP1.2 <400> SEQUENCE: 588 caaccaucac ucuguucug 19 <210> SEQ ID NO 589 <211> LENGTH: 21 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - mTCPTP1.2 <220> FEATURE: <221> NAME/KEY: misc_feature <222> LOCATION: 20, 21 <223> OTHER INFORMATION: n = A,T,C,G or U <400> SEQUENCE: 589 cagaacagag ugaugguugn n 21 <210> SEQ ID NO 590 <211> LENGTH: 21 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - mTCPTP1.2 <220> FEATURE: <221> NAME/KEY: misc_feature <222> LOCATION: 1, 2 <223> OTHER INFORMATION: n = A,T,C,G or U <400> SEQUENCE: 590 nncaaccauc acucuguucu g 21 <210> SEQ ID NO 591 <211> LENGTH: 36 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Oligonucleotide primer (TC45 5′ BamHI) <400> SEQUENCE: 591 ggggggatcc atgcccacca ccatcgagcg ggagtt 36 <210> SEQ ID NO 592 <211> LENGTH: 49 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Oligonucleotide primer (TC45 3′ EcoRI) <400> SEQUENCE: 592 ggggaattct taggtgtctg tcaatcttgg cctttttctt tttcgttca 49 <210> SEQ ID NO 593 <211> LENGTH: 21 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - hTCPTP1.4 <400> SEQUENCE: 593 guugucaugc ugaaccgcat t 21 <210> SEQ ID NO 594 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - hTCPTP1.4 <400> SEQUENCE: 594 guugucaugc ugaaccgca 19 <210> SEQ ID NO 595 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - hTCPTP1.4 <400> SEQUENCE: 595 ugcgguucag caugacaac 19 <210> SEQ ID NO 596 <211> LENGTH: 21 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - hTCPTP1.4 <220> FEATURE: <221> NAME/KEY: misc_feature <222> LOCATION: 20, 21 <223> OTHER INFORMATION: n = A,T,C,G or U <400> SEQUENCE: 596 guugucaugc ugaaccgcan n 21 <210> SEQ ID NO 597 <211> LENGTH: 21 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - hTCPTP1.4 <220> FEATURE: <221> NAME/KEY: misc_feature <222> LOCATION: 1, 2 <223> OTHER INFORMATION: n = A,T,C,G or U <400> SEQUENCE: 597 nnugcgguuc agcaugacaa c 21 <210> SEQ ID NO 598 <211> LENGTH: 21 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - hTCPTP1.5 <400> SEQUENCE: 598 gcccauauga ucacagucgt g 21 <210> SEQ ID NO 599 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - hTCPTP1.5 <400> SEQUENCE: 599 gcccauauga ucacagucg 19 <210> SEQ ID NO 600 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - hTCPTP1.5 <400> SEQUENCE: 600 cgacugugau cauaugggc 19 <210> SEQ ID NO 601 <211> LENGTH: 21 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - hTCPTP1.5 <220> FEATURE: <221> NAME/KEY: misc_feature <222> LOCATION: 20, 21 <223> OTHER INFORMATION: n = A,T,C,G or U <400> SEQUENCE: 601 gcccauauga ucacagucgn n 21 <210> SEQ ID NO 602 <211> LENGTH: 21 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - hTCPTP1.5 <220> FEATURE: <221> NAME/KEY: misc_feature <222> LOCATION: 1, 2 <223> OTHER INFORMATION: n = A,T,C,G or U <400> SEQUENCE: 602 nncgacugug aucauauggg c 21 <210> SEQ ID NO 603 <211> LENGTH: 21 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - hTCPTP1.6 <400> SEQUENCE: 603 ucgguuaaau gugcacagua c 21 <210> SEQ ID NO 604 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - hTCPTP1.6 <400> SEQUENCE: 604 ucgguuaaau gugcacagu 19 <210> SEQ ID NO 605 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - hTCPTP1.6 <400> SEQUENCE: 605 acugugcaca uuuaaccga 19 <210> SEQ ID NO 606 <211> LENGTH: 21 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - hTCPTP1.6 <220> FEATURE: <221> NAME/KEY: misc_feature <222> LOCATION: 20, 21 <223> OTHER INFORMATION: n = A,T,C,G or U <400> SEQUENCE: 606 ucgguuaaau gugcacagun n 21 <210> SEQ ID NO 607 <211> LENGTH: 21 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - hTCPTP1.6 <220> FEATURE: <221> NAME/KEY: misc_feature <222> LOCATION: 1, 2 <223> OTHER INFORMATION: n = A,T,C,G or U <400> SEQUENCE: 607 nnacugugca cauuuaaccg a 21 <210> SEQ ID NO 608 <211> LENGTH: 21 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - hTCPTP1.7 <400> SEQUENCE: 608 ugacuauccu cauagagugg g 21 <210> SEQ ID NO 609 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - hTCPTP1.7 <400> SEQUENCE: 609 ugacuauccu cauagagug 19 <210> SEQ ID NO 610 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - hTCPTP1.7 <400> SEQUENCE: 610 cacucuauga ggauaguca 19 <210> SEQ ID NO 611 <211> LENGTH: 21 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - hTCPTP1.7 <220> FEATURE: <221> NAME/KEY: misc_feature <222> LOCATION: 20, 21 <223> OTHER INFORMATION: n = A,T,C,G or U <400> SEQUENCE: 611 ugacuauccu cauagagugn n 21 <210> SEQ ID NO 612 <211> LENGTH: 21 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - hTCPTP1.7 <220> FEATURE: <221> NAME/KEY: misc_feature <222> LOCATION: 1, 2 <223> OTHER INFORMATION: n = A,T,C,G or U <400> SEQUENCE: 612 nncacucuau gaggauaguc a 21 <210> SEQ ID NO 613 <211> LENGTH: 21 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - hTCPTP1.1 <400> SEQUENCE: 613 agugagagaa ucuggcucct t 21 <210> SEQ ID NO 614 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - hTCPTP1.1 <400> SEQUENCE: 614 agugagagaa ucuggcucc 19 <210> SEQ ID NO 615 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - hTCPTP1.1 <400> SEQUENCE: 615 ggagccagau ucucucacu 19 <210> SEQ ID NO 616 <211> LENGTH: 21 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - hTCPTP1.1 <220> FEATURE: <221> NAME/KEY: misc_feature <222> LOCATION: 20, 21 <223> OTHER INFORMATION: n = A,T,C,G or U <400> SEQUENCE: 616 agugagagaa ucuggcuccn n 21 <210> SEQ ID NO 617 <211> LENGTH: 21 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - hTCPTP1.1 <220> FEATURE: <221> NAME/KEY: misc_feature <222> LOCATION: 1, 2 <223> OTHER INFORMATION: n = A,T,C,G or U <400> SEQUENCE: 617 nnggagccag auucucucac u 21 <210> SEQ ID NO 618 <211> LENGTH: 21 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - hTCPTP1.2 <400> SEQUENCE: 618 ggaagacuua ucuccugcct t 21 <210> SEQ ID NO 619 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - hTCPTP1.2 <400> SEQUENCE: 619 ggaagacuua ucuccugcc 19 <210> SEQ ID NO 620 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - hTCPTP1.2 <400> SEQUENCE: 620 ggcaggagau aagucuucc 19 <210> SEQ ID NO 621 <211> LENGTH: 21 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - hTCPTP1.2 <220> FEATURE: <221> NAME/KEY: misc_feature <222> LOCATION: 20, 21 <223> OTHER INFORMATION: n = A,T,C,G or U <400> SEQUENCE: 621 ggaagacuua ucuccugccn n 21 <210> SEQ ID NO 622 <211> LENGTH: 21 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - hTCPTP1.2 <220> FEATURE: <221> NAME/KEY: misc_feature <222> LOCATION: 1, 2 <223> OTHER INFORMATION: n = A,T,C,G or U <400> SEQUENCE: 622 nnggcaggag auaagucuuc c 21 <210> SEQ ID NO 623 <211> LENGTH: 21 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - hTCPTP1.3 <400> SEQUENCE: 623 ggugaccgau guacaggact t 21 <210> SEQ ID NO 624 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - hTCPTP1.3 <400> SEQUENCE: 624 ggugaccgau guacaggac 19 <210> SEQ ID NO 625 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - hTCPTP1.3 <400> SEQUENCE: 625 guccuguaca ucggucacc 19 <210> SEQ ID NO 626 <211> LENGTH: 21 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - hTCPTP1.3 <220> FEATURE: <221> NAME/KEY: misc_feature <222> LOCATION: 20, 21 <223> OTHER INFORMATION: n = A,T,C,G or U <400> SEQUENCE: 626 ggugaccgau guacaggacn n 21 <210> SEQ ID NO 627 <211> LENGTH: 21 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - hTCPTP1.3 <220> FEATURE: <221> NAME/KEY: misc_feature <222> LOCATION: 1, 2 <223> OTHER INFORMATION: n = A,T,C,G or U <400> SEQUENCE: 627 nnguccugua caucggucac c 21 <210> SEQ ID NO 628 <211> LENGTH: 50 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Hairpin vector - hPTP1B H1.2-HP4 <400> SEQUENCE: 628 tttgcccaaa ggagttacat tcgtaagaat gtaactcctt tgggcttttt 50 <210> SEQ ID NO 629 <211> LENGTH: 50 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Hairpin vector - hPTP1B H1.2-HP4 <400> SEQUENCE: 629 ctagaaaaag cccaaaggag ttacattctt acgaatgtaa ctcctttggg 50 <210> SEQ ID NO 630 <211> LENGTH: 50 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Hairpin vector - hPTP1B H1.2-HP4 <400> SEQUENCE: 630 uuugcccaaa ggaguuacau ucguaagaau guaacuccuu ugggcuuuuu 50 <210> SEQ ID NO 631 <211> LENGTH: 50 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Hairpin vector - hPTP1B H1.2-HP4 <400> SEQUENCE: 631 cuagaaaaag cccaaaggag uuacauucuu acgaauguaa cuccuuuggg 50 <210> SEQ ID NO 632 <211> LENGTH: 55 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Hairpin vector - hPTP1B H1.2-HP9 <400> SEQUENCE: 632 tttgcccaaa ggagttacat tccctgggta agaatgtaac tcctttgggc ttttt 55 <210> SEQ ID NO 633 <211> LENGTH: 55 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Hairpin vector - hPTP1B H1.2-HP9 <400> SEQUENCE: 633 ctagaaaaag cccaaaggag ttacattctt acccagggaa tgtaactcct ttggg 55 <210> SEQ ID NO 634 <211> LENGTH: 55 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Hairpin vector - hPTP1B H1.2-HP9 <400> SEQUENCE: 634 uuugcccaaa ggaguuacau ucccugggua agaauguaac uccuuugggc uuuuu 55 <210> SEQ ID NO 635 <211> LENGTH: 55 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Hairpin vector - hPTP1B H1.2-HP9 <400> SEQUENCE: 635 cuagaaaaag cccaaaggag uuacauucuu acccagggaa uguaacuccu uuggg 55 <210> SEQ ID NO 636 <211> LENGTH: 50 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Hairpin vector - mPTP1B M1.1-HP4 <400> SEQUENCE: 636 tttgaagccc agaggagcta taagaatata gctcctctgg gcttcttttt 50 <210> SEQ ID NO 637 <211> LENGTH: 50 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Hairpin vector - mPTP1B M1.1-HP4 <400> SEQUENCE: 637 ctagaaaaag aagcccagag gagctatatt cttatagctc ctctgggctt 50 <210> SEQ ID NO 638 <211> LENGTH: 50 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Hairpin vector - mPTP1B M1.1-HP4 <400> SEQUENCE: 638 uuugaagccc agaggagcua uaagaauaua gcuccucugg gcuucuuuuu 50 <210> SEQ ID NO 639 <211> LENGTH: 50 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Hairpin vector - mPTP1B M1.1-HP4 <400> SEQUENCE: 639 cuagaaaaag aagcccagag gagcuauauu cuuauagcuc cucugggcuu 50 <210> SEQ ID NO 640 <211> LENGTH: 55 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Hairpin vector - mPTP1B M1.1-HP9 <400> SEQUENCE: 640 tttgaagccc agaggagcta tagggtgaga atatagctcc tctgggcttc ttttt 55 <210> SEQ ID NO 641 <211> LENGTH: 55 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Hairpin vector - mPTP1B M1.1-HP9 <400> SEQUENCE: 641 ctagaaaaag aagcccagag gagctatatt ctcaccctat agctcctctg ggctt 55 <210> SEQ ID NO 642 <211> LENGTH: 55 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Hairpin vector - mPTP1B M1.1-HP9 <400> SEQUENCE: 642 uuugaagccc agaggagcua uagggugaga auauagcucc ucugggcuuc uuuuu 55 <210> SEQ ID NO 643 <211> LENGTH: 55 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Hairpin vector - mPTP1B M1.1-HP9 <400> SEQUENCE: 643 cuagaaaaag aagcccagag gagcuauauu cucacccuau agcuccucug ggcuu 55 <210> SEQ ID NO 644 <211> LENGTH: 21 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Oligonucleotide selected from scanning open reading frame of TC45 mRNA <400> SEQUENCE: 644 aacagauaca gagauguaag c 21 <210> SEQ ID NO 645 <211> LENGTH: 21 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Oligonucleotide selected from scanning open reading frame of TC45 mRNA <400> SEQUENCE: 645 aagcccauau gaucacaguc g 21 <210> SEQ ID NO 646 <211> LENGTH: 21 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interefering RNA - DSP3.4 <400> SEQUENCE: 646 ggugacacau auucugucut t 21 <210> SEQ ID NO 647 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interefering RNA - DSP3.4 <400> SEQUENCE: 647 ggugacacau auucugucu 19 <210> SEQ ID NO 648 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interefering RNA - DSP3.4 <400> SEQUENCE: 648 agacagaaua ugugucacc 19 <210> SEQ ID NO 649 <211> LENGTH: 21 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interefering RNA - DSP3.4 <220> FEATURE: <221> NAME/KEY: misc_feature <222> LOCATION: 20, 21 <223> OTHER INFORMATION: n = A,T,C,G or U <400> SEQUENCE: 649 ggugacacau auucugucun n 21 <210> SEQ ID NO 650 <211> LENGTH: 21 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interefering RNA - DSP3.4 <220> FEATURE: <221> NAME/KEY: misc_feature <222> LOCATION: 1, 2 <223> OTHER INFORMATION: n = A,T,C,G or U <400> SEQUENCE: 650 nnagacagaa uaugugucac c 21 <210> SEQ ID NO 651 <211> LENGTH: 21 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interefering RNA - DHFR.1 <400> SEQUENCE: 651 gaccugguuc uccauuccut t 21 <210> SEQ ID NO 652 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interefering RNA - DHFR.1 <400> SEQUENCE: 652 gaccugguuc uccauuccu 19 <210> SEQ ID NO 653 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interefering RNA - DHFR.1 <400> SEQUENCE: 653 aggaauggag aaccagguc 19 <210> SEQ ID NO 654 <211> LENGTH: 21 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interefering RNA - DHFR.1 <220> FEATURE: <221> NAME/KEY: misc_feature <222> LOCATION: 20, 21 <223> OTHER INFORMATION: n = A,T,C,G or U <400> SEQUENCE: 654 gaccugguuc uccauuccun n 21 <210> SEQ ID NO 655 <211> LENGTH: 21 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interefering RNA - DHFR.1 <220> FEATURE: <221> NAME/KEY: misc_feature <222> LOCATION: 1, 2 <223> OTHER INFORMATION: n = A,T,C,G or U <400> SEQUENCE: 655 nnaggaaugg agaaccaggu c 21 <210> SEQ ID NO 656 <211> LENGTH: 21 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interefering RNA - DHFR.3 <400> SEQUENCE: 656 gcaguguauu ugcuagguct t 21 <210> SEQ ID NO 657 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interefering RNA - DHFR.3 <400> SEQUENCE: 657 gcaguguauu ugcuagguc 19 <210> SEQ ID NO 658 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interefering RNA - DHFR.3 <400> SEQUENCE: 658 gaccuagcaa auacacugc 19 <210> SEQ ID NO 659 <211> LENGTH: 21 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interefering RNA - DHFR.3 <220> FEATURE: <221> NAME/KEY: misc_feature <222> LOCATION: 20, 21 <223> OTHER INFORMATION: n = A,T,C,G or U <400> SEQUENCE: 659 gcaguguauu ugcuaggucn n 21 <210> SEQ ID NO 660 <211> LENGTH: 21 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interefering RNA - DHFR.3 <220> FEATURE: <221> NAME/KEY: misc_feature <222> LOCATION: 1, 2 <223> OTHER INFORMATION: n = A,T,C,G or U <400> SEQUENCE: 660 nngaccuagc aaauacacug c 21 <210> SEQ ID NO 661 <211> LENGTH: 21 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interefering RNA - DHFR.4 <400> SEQUENCE: 661 gucagcgagc agguucucat t 21 <210> SEQ ID NO 662 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interefering RNA - DHFR.4 <400> SEQUENCE: 662 gucagcgagc agguucuca 19 <210> SEQ ID NO 663 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interefering RNA - DHFR.4 <400> SEQUENCE: 663 ugagaaccug cucgcugac 19 <210> SEQ ID NO 664 <211> LENGTH: 21 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interefering RNA - DHFR.4 <220> FEATURE: <221> NAME/KEY: misc_feature <222> LOCATION: 20, 21 <223> OTHER INFORMATION: n = A,T,C,G or U <400> SEQUENCE: 664 gucagcgagc agguucucan n 21 <210> SEQ ID NO 665 <211> LENGTH: 21 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interefering RNA - DHFR.4 <220> FEATURE: <221> NAME/KEY: misc_feature <222> LOCATION: 1, 2 <223> OTHER INFORMATION: n = A,T,C,G or U <400> SEQUENCE: 665 nnugagaacc ugcucgcuga c 21 <210> SEQ ID NO 666 <211> LENGTH: 21 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interefering RNA - TYMS.1 <400> SEQUENCE: 666 ccaaacgugu guucuggaat t 21 <210> SEQ ID NO 667 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interefering RNA - TYMS.1 <400> SEQUENCE: 667 ccaaacgugu guucuggaa 19 <210> SEQ ID NO 668 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interefering RNA - TYMS.1 <400> SEQUENCE: 668 uuccagaaca cacguuugg 19 <210> SEQ ID NO 669 <211> LENGTH: 21 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interefering RNA - TYMS.1 <220> FEATURE: <221> NAME/KEY: misc_feature <222> LOCATION: 20, 21 <223> OTHER INFORMATION: n = A,T,C,G or U <400> SEQUENCE: 669 ccaaacgugu guucuggaan n 21 <210> SEQ ID NO 670 <211> LENGTH: 21 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interefering RNA - TYMS.1 <220> FEATURE: <221> NAME/KEY: misc_feature <222> LOCATION: 1, 2 <223> OTHER INFORMATION: n = A,T,C,G or U <400> SEQUENCE: 670 nnuuccagaa cacacguuug g 21 <210> SEQ ID NO 671 <211> LENGTH: 21 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interefering RNA - TYMS.2 <400> SEQUENCE: 671 ccaacccuga cgacagaagt t 21 <210> SEQ ID NO 672 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interefering RNA - TYMS.2 <400> SEQUENCE: 672 ccaacccuga cgacagaag 19 <210> SEQ ID NO 673 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interefering RNA - TYMS.2 <400> SEQUENCE: 673 cuucugucgu caggguugg 19 <210> SEQ ID NO 674 <211> LENGTH: 21 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interefering RNA - TYMS.2 <220> FEATURE: <221> NAME/KEY: misc_feature <222> LOCATION: 20, 21 <223> OTHER INFORMATION: n = A,T,C,G or U <400> SEQUENCE: 674 ccaacccuga cgacagaagn n 21 <210> SEQ ID NO 675 <211> LENGTH: 21 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interefering RNA - TYMS.2 <220> FEATURE: <221> NAME/KEY: misc_feature <222> LOCATION: 1, 2 <223> OTHER INFORMATION: n = A,T,C,G or U <400> SEQUENCE: 675 nncuucuguc gucaggguug g 21 <210> SEQ ID NO 676 <211> LENGTH: 21 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interefering RNA - TYMS.3 <400> SEQUENCE: 676 gccaggugac uuuauacact t 21 <210> SEQ ID NO 677 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interefering RNA - TYMS.3 <400> SEQUENCE: 677 gccaggugac uuuauacac 19 <210> SEQ ID NO 678 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interefering RNA - TYMS.3 <400> SEQUENCE: 678 guguauaaag ucaccuggc 19 <210> SEQ ID NO 679 <211> LENGTH: 21 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interefering RNA - TYMS.3 <220> FEATURE: <221> NAME/KEY: misc_feature <222> LOCATION: 20, 21 <223> OTHER INFORMATION: n = A,T,C,G or U <400> SEQUENCE: 679 gccaggugac uuuauacacn n 21 <210> SEQ ID NO 680 <211> LENGTH: 21 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interefering RNA - TYMS.3 <220> FEATURE: <221> NAME/KEY: misc_feature <222> LOCATION: 1, 2 <223> OTHER INFORMATION: n = A,T,C,G or U <400> SEQUENCE: 680 nnguguauaa agucaccugg c 21 <210> SEQ ID NO 681 <211> LENGTH: 21 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interefering RNA - TYMS.4 <400> SEQUENCE: 681 cccagaccuu ucccaaagct t 21 <210> SEQ ID NO 682 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interefering RNA - TYMS.4 <400> SEQUENCE: 682 cccagaccuu ucccaaagc 19 <210> SEQ ID NO 683 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interefering RNA - TYMS.4 <400> SEQUENCE: 683 gcuuugggaa aggucuggg 19 <210> SEQ ID NO 684 <211> LENGTH: 21 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interefering RNA - TYMS.4 <220> FEATURE: <221> NAME/KEY: misc_feature <222> LOCATION: 20, 21 <223> OTHER INFORMATION: n = A,T,C,G or U <400> SEQUENCE: 684 cccagaccuu ucccaaagcn n 21 <210> SEQ ID NO 685 <211> LENGTH: 21 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interefering RNA - TYMS.4 <220> FEATURE: <221> NAME/KEY: misc_feature <222> LOCATION: 1, 2 <223> OTHER INFORMATION: n = A,T,C,G or U <400> SEQUENCE: 685 nngcuuuggg aaaggucugg g 21 <210> SEQ ID NO 686 <211> LENGTH: 21 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interefering RNA - TOP1.1 <400> SEQUENCE: 686 gauagagccu ccuggacuut t 21 <210> SEQ ID NO 687 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interefering RNA - TOP1.1 <400> SEQUENCE: 687 gauagagccu ccuggacuu 19 <210> SEQ ID NO 688 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interefering RNA - TOP1.1 <400> SEQUENCE: 688 aaguccagga ggcucuauc 19 <210> SEQ ID NO 689 <211> LENGTH: 21 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interefering RNA - TOP1.1 <220> FEATURE: <221> NAME/KEY: misc_feature <222> LOCATION: 20, 21 <223> OTHER INFORMATION: n = A,T,C,G or U <400> SEQUENCE: 689 gauagagccu ccuggacuun n 21 <210> SEQ ID NO 690 <211> LENGTH: 21 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interefering RNA - TOP1.1 <220> FEATURE: <221> NAME/KEY: misc_feature <222> LOCATION: 1, 2 <223> OTHER INFORMATION: n = A,T,C,G or U <400> SEQUENCE: 690 nnaaguccag gaggcucuau c 21 <210> SEQ ID NO 691 <211> LENGTH: 21 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interefering RNA - TOP1.2 <400> SEQUENCE: 691 guccggcaug auaacaaggt t 21 <210> SEQ ID NO 692 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interefering RNA - TOP1.2 <400> SEQUENCE: 692 guccggcaug auaacaagg 19 <210> SEQ ID NO 693 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interefering RNA - TOP1.2 <400> SEQUENCE: 693 ccuuguuauc augccggac 19 <210> SEQ ID NO 694 <211> LENGTH: 21 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interefering RNA - TOP1.2 <220> FEATURE: <221> NAME/KEY: misc_feature <222> LOCATION: 20, 21 <223> OTHER INFORMATION: n = A,T,C,G or U <400> SEQUENCE: 694 guccggcaug auaacaaggn n 21 <210> SEQ ID NO 695 <211> LENGTH: 21 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interefering RNA - TOP1.2 <220> FEATURE: <221> NAME/KEY: misc_feature <222> LOCATION: 1, 2 <223> OTHER INFORMATION: n = A,T,C,G or U <400> SEQUENCE: 695 nnccuuguua ucaugccgga c 21 <210> SEQ ID NO 696 <211> LENGTH: 21 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interefering RNA - TOP1.3 <400> SEQUENCE: 696 ggagaaacag cggacacugt t 21 <210> SEQ ID NO 697 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interefering RNA - TOP1.3 <400> SEQUENCE: 697 ggagaaacag cggacacug 19 <210> SEQ ID NO 698 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interefering RNA - TOP1.3 <400> SEQUENCE: 698 caguguccgc uguuucucc 19 <210> SEQ ID NO 699 <211> LENGTH: 21 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interefering RNA - TOP1.3 <220> FEATURE: <221> NAME/KEY: misc_feature <222> LOCATION: 20, 21 <223> OTHER INFORMATION: n = A,T,C,G or U <400> SEQUENCE: 699 ggagaaacag cggacacugn n 21 <210> SEQ ID NO 700 <211> LENGTH: 21 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interefering RNA - TOP1.3 <220> FEATURE: <221> NAME/KEY: misc_feature <222> LOCATION: 1, 2 <223> OTHER INFORMATION: n = A,T,C,G or U <400> SEQUENCE: 700 nncagugucc gcuguuucuc c 21 <210> SEQ ID NO 701 <211> LENGTH: 21 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interefering RNA - TOP1.4 <400> SEQUENCE: 701 gcagcccgag gaugaucuut t 21 <210> SEQ ID NO 702 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interefering RNA - TOP1.4 <400> SEQUENCE: 702 gcagcccgag gaugaucuu 19 <210> SEQ ID NO 703 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interefering RNA - TOP1.4 <400> SEQUENCE: 703 aagaucaucc ucgggcugc 19 <210> SEQ ID NO 704 <211> LENGTH: 21 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interefering RNA - TOP1.4 <220> FEATURE: <221> NAME/KEY: misc_feature <222> LOCATION: 20, 21 <223> OTHER INFORMATION: n = A,T,C,G or U <400> SEQUENCE: 704 gcagcccgag gaugaucuun n 21 <210> SEQ ID NO 705 <211> LENGTH: 21 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interefering RNA - TOP1.4 <220> FEATURE: <221> NAME/KEY: misc_feature <222> LOCATION: 1, 2 <223> OTHER INFORMATION: n = A,T,C,G or U <400> SEQUENCE: 705 nnaagaucau ccucgggcug c 21 <210> SEQ ID NO 706 <211> LENGTH: 21 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interefering RNA - IKK.1 <400> SEQUENCE: 706 gagucuccuc uggggaagct t 21 <210> SEQ ID NO 707 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interefering RNA - IKK.1 <400> SEQUENCE: 707 gagucuccuc uggggaagc 19 <210> SEQ ID NO 708 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interefering RNA - IKK.1 <400> SEQUENCE: 708 gcuuccccag aggagacuc 19 <210> SEQ ID NO 709 <211> LENGTH: 21 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interefering RNA - IKK.1 <220> FEATURE: <221> NAME/KEY: misc_feature <222> LOCATION: 20, 21 <223> OTHER INFORMATION: n = A,T,C,G or U <400> SEQUENCE: 709 gagucuccuc uggggaagcn n 21 <210> SEQ ID NO 710 <211> LENGTH: 21 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interefering RNA - IKK.1 <220> FEATURE: <221> NAME/KEY: misc_feature <222> LOCATION: 1, 2 <223> OTHER INFORMATION: n = A,T,C,G or U <400> SEQUENCE: 710 nngcuucccc agaggagacu c 21 <210> SEQ ID NO 711 <211> LENGTH: 21 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interefering RNA - IKK.2 <400> SEQUENCE: 711 ggaguuccuc augugcaagt t 21 <210> SEQ ID NO 712 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interefering RNA - IKK.2 <400> SEQUENCE: 712 ggaguuccuc augugcaag 19 <210> SEQ ID NO 713 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interefering RNA - IKK.2 <400> SEQUENCE: 713 cuugcacaug aggaacucc 19 <210> SEQ ID NO 714 <211> LENGTH: 21 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interefering RNA - IKK.2 <220> FEATURE: <221> NAME/KEY: misc_feature <222> LOCATION: 20, 21 <223> OTHER INFORMATION: n = A,T,C,G or U <400> SEQUENCE: 714 ggaguuccuc augugcaagn n 21 <210> SEQ ID NO 715 <211> LENGTH: 21 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interefering RNA - IKK.2 <220> FEATURE: <221> NAME/KEY: misc_feature <222> LOCATION: 1, 2 <223> OTHER INFORMATION: n = A,T,C,G or U <400> SEQUENCE: 715 nncuugcaca ugaggaacuc c 21 <210> SEQ ID NO 716 <211> LENGTH: 21 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interefering RNA - IKK.3 <400> SEQUENCE: 716 ggccucugug aaagcccagt t 21 <210> SEQ ID NO 717 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interefering RNA - IKK.3 <400> SEQUENCE: 717 ggccucugug aaagcccag 19 <210> SEQ ID NO 718 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interefering RNA - IKK.3 <400> SEQUENCE: 718 cugggcuuuc acagaggcc 19 <210> SEQ ID NO 719 <211> LENGTH: 21 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interefering RNA - IKK.3 <220> FEATURE: <221> NAME/KEY: misc_feature <222> LOCATION: 20, 21 <223> OTHER INFORMATION: n = A,T,C,G or U <400> SEQUENCE: 719 ggccucugug aaagcccagn n 21 <210> SEQ ID NO 720 <211> LENGTH: 21 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interefering RNA - IKK.3 <220> FEATURE: <221> NAME/KEY: misc_feature <222> LOCATION: 1, 2 <223> OTHER INFORMATION: n = A,T,C,G or U <400> SEQUENCE: 720 nncugggcuu ucacagaggc c 21 <210> SEQ ID NO 721 <211> LENGTH: 21 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interefering RNA - IKK.4 <400> SEQUENCE: 721 cacgcugcuc uugauguggt t 21 <210> SEQ ID NO 722 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interefering RNA - IKK.4 <400> SEQUENCE: 722 cacgcugcuc uugaugugg 19 <210> SEQ ID NO 723 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interefering RNA - IKK.4 <400> SEQUENCE: 723 ccacaucaag agcagcgug 19 <210> SEQ ID NO 724 <211> LENGTH: 21 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interefering RNA - IKK.4 <220> FEATURE: <221> NAME/KEY: misc_feature <222> LOCATION: 20, 21 <223> OTHER INFORMATION: n = A,T,C,G or U <400> SEQUENCE: 724 cacgcugcuc uugauguggn n 21 <210> SEQ ID NO 725 <211> LENGTH: 21 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interefering RNA - IKK.4 <220> FEATURE: <221> NAME/KEY: misc_feature <222> LOCATION: 1, 2 <223> OTHER INFORMATION: n = A,T,C,G or U <400> SEQUENCE: 725 nnccacauca agagcagcgu g 21 <210> SEQ ID NO 726 <211> LENGTH: 21 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interefering RNA - MKK4.1 <400> SEQUENCE: 726 gugggcaaau aauggcagut t 21 <210> SEQ ID NO 727 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interefering RNA - MKK4.1 <400> SEQUENCE: 727 gugggcaaau aauggcagu 19 <210> SEQ ID NO 728 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interefering RNA - MKK4.1 <400> SEQUENCE: 728 acugccauua uuugcccac 19 <210> SEQ ID NO 729 <211> LENGTH: 21 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interefering RNA - MKK4.1 <220> FEATURE: <221> NAME/KEY: misc_feature <222> LOCATION: 20, 21 <223> OTHER INFORMATION: n = A,T,C,G or U <400> SEQUENCE: 729 gugggcaaau aauggcagun n 21 <210> SEQ ID NO 730 <211> LENGTH: 21 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interefering RNA - MKK4.1 <220> FEATURE: <221> NAME/KEY: misc_feature <222> LOCATION: 1, 2 <223> OTHER INFORMATION: n = A,T,C,G or U <400> SEQUENCE: 730 nnacugccau uauuugccca c 21 <210> SEQ ID NO 731 <211> LENGTH: 21 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interefering RNA - MKK4.2 <400> SEQUENCE: 731 cugugaaagc acuaaaccat t 21 <210> SEQ ID NO 732 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interefering RNA - MKK4.2 <400> SEQUENCE: 732 cugugaaagc acuaaacca 19 <210> SEQ ID NO 733 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interefering RNA - MKK4.2 <400> SEQUENCE: 733 ugguuuagug cuuucacag 19 <210> SEQ ID NO 734 <211> LENGTH: 21 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interefering RNA - MKK4.2 <220> FEATURE: <221> NAME/KEY: misc_feature <222> LOCATION: 20, 21 <223> OTHER INFORMATION: n = A,T,C,G or U <400> SEQUENCE: 734 cugugaaagc acuaaaccan n 21 <210> SEQ ID NO 735 <211> LENGTH: 21 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interefering RNA - MKK4.2 <220> FEATURE: <221> NAME/KEY: misc_feature <222> LOCATION: 1, 2 <223> OTHER INFORMATION: n = A,T,C,G or U <400> SEQUENCE: 735 nnugguuuag ugcuuucaca g 21 <210> SEQ ID NO 736 <211> LENGTH: 21 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interefering RNA - MKK4.3 <400> SEQUENCE: 736 ggagauccuc cgcagcugat t 21 <210> SEQ ID NO 737 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interefering RNA - MKK4.3 <400> SEQUENCE: 737 ggagauccuc cgcagcuga 19 <210> SEQ ID NO 738 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interefering RNA - MKK4.3 <400> SEQUENCE: 738 ucagcugcgg aggaucucc 19 <210> SEQ ID NO 739 <211> LENGTH: 21 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interefering RNA - MKK4.3 <220> FEATURE: <221> NAME/KEY: misc_feature <222> LOCATION: 20, 21 <223> OTHER INFORMATION: n = A,T,C,G or U <400> SEQUENCE: 739 ggagauccuc cgcagcugan n 21 <210> SEQ ID NO 740 <211> LENGTH: 21 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interefering RNA - MKK4.3 <220> FEATURE: <221> NAME/KEY: misc_feature <222> LOCATION: 1, 2 <223> OTHER INFORMATION: n = A,T,C,G or U <400> SEQUENCE: 740 nnucagcugc ggaggaucuc c 21 <210> SEQ ID NO 741 <211> LENGTH: 21 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interefering RNA - MKK4.4 <400> SEQUENCE: 741 gcucuuuaua cuuuggccut t 21 <210> SEQ ID NO 742 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interefering RNA - MKK4.4 <400> SEQUENCE: 742 gcucuuuaua cuuuggccu 19 <210> SEQ ID NO 743 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interefering RNA - MKK4.4 <400> SEQUENCE: 743 aggccaaagu auaaagagc 19 <210> SEQ ID NO 744 <211> LENGTH: 21 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interefering RNA - MKK4.4 <220> FEATURE: <221> NAME/KEY: misc_feature <222> LOCATION: 20, 21 <223> OTHER INFORMATION: n = A,T,C,G or U <400> SEQUENCE: 744 gcucuuuaua cuuuggccun n 21 <210> SEQ ID NO 745 <211> LENGTH: 21 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interefering RNA - MKK4.4 <220> FEATURE: <221> NAME/KEY: misc_feature <222> LOCATION: 1, 2 <223> OTHER INFORMATION: n = A,T,C,G or U <400> SEQUENCE: 745 nnaggccaaa guauaaagag c 21 <210> SEQ ID NO 746 <211> LENGTH: 21 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interefering RNA - MKK7.1 <400> SEQUENCE: 746 gcagacgggc uaccugacct t 21 <210> SEQ ID NO 747 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interefering RNA - MKK7.1 <400> SEQUENCE: 747 gcagacgggc uaccugacc 19 <210> SEQ ID NO 748 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interefering RNA - MKK7.1 <400> SEQUENCE: 748 ggucagguag cccgucugc 19 <210> SEQ ID NO 749 <211> LENGTH: 21 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interefering RNA - MKK7.1 <220> FEATURE: <221> NAME/KEY: misc_feature <222> LOCATION: 20, 21 <223> OTHER INFORMATION: n = A,T,C,G or U <400> SEQUENCE: 749 gcagacgggc uaccugaccn n 21 <210> SEQ ID NO 750 <211> LENGTH: 21 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interefering RNA - MKK7.1 <220> FEATURE: <221> NAME/KEY: misc_feature <222> LOCATION: 1, 2 <223> OTHER INFORMATION: n = A,T,C,G or U <400> SEQUENCE: 750 nnggucaggu agcccgucug c 21 <210> SEQ ID NO 751 <211> LENGTH: 21 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interefering RNA - MKK7.2 <400> SEQUENCE: 751 cacggacguc uucaucgcct t 21 <210> SEQ ID NO 752 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interefering RNA - MKK7.2 <400> SEQUENCE: 752 cacggacguc uucaucgcc 19 <210> SEQ ID NO 753 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interefering RNA - MKK7.2 <400> SEQUENCE: 753 ggcgaugaag acguccgug 19 <210> SEQ ID NO 754 <211> LENGTH: 21 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interefering RNA - MKK7.2 <220> FEATURE: <221> NAME/KEY: misc_feature <222> LOCATION: 20, 21 <223> OTHER INFORMATION: n = A,T,C,G or U <400> SEQUENCE: 754 cacggacguc uucaucgccn n 21 <210> SEQ ID NO 755 <211> LENGTH: 21 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interefering RNA - MKK7.2 <220> FEATURE: <221> NAME/KEY: misc_feature <222> LOCATION: 1, 2 <223> OTHER INFORMATION: n = A,T,C,G or U <400> SEQUENCE: 755 nnggcgauga agacguccgu g 21 <210> SEQ ID NO 756 <211> LENGTH: 21 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interefering RNA - MKK7.3 <400> SEQUENCE: 756 gaagcggaug cagggcccct t 21 <210> SEQ ID NO 757 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interefering RNA - MKK7.3 <400> SEQUENCE: 757 gaagcggaug cagggcccc 19 <210> SEQ ID NO 758 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interefering RNA - MKK7.3 <400> SEQUENCE: 758 ggggcccugc auccgcuuc 19 <210> SEQ ID NO 759 <211> LENGTH: 21 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interefering RNA - MKK7.3 <220> FEATURE: <221> NAME/KEY: misc_feature <222> LOCATION: 20, 21 <223> OTHER INFORMATION: n = A,T,C,G or U <400> SEQUENCE: 759 gaagcggaug cagggccccn n 21 <210> SEQ ID NO 760 <211> LENGTH: 21 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interefering RNA - MKK7.3 <220> FEATURE: <221> NAME/KEY: misc_feature <222> LOCATION: 1, 2 <223> OTHER INFORMATION: n = A,T,C,G or U <400> SEQUENCE: 760 nnggggcccu gcauccgcuu c 21 <210> SEQ ID NO 761 <211> LENGTH: 21 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interefering RNA - MKK7.4 <400> SEQUENCE: 761 cugcaagacg gacuuugagt t 21 <210> SEQ ID NO 762 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interefering RNA - MKK7.4 <400> SEQUENCE: 762 cugcaagacg gacuuugag 19 <210> SEQ ID NO 763 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interefering RNA - MKK7.4 <400> SEQUENCE: 763 cucaaagucc gucuugcag 19 <210> SEQ ID NO 764 <211> LENGTH: 21 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interefering RNA - MKK7.4 <220> FEATURE: <221> NAME/KEY: misc_feature <222> LOCATION: 20, 21 <223> OTHER INFORMATION: n = A,T,C,G or U <400> SEQUENCE: 764 cugcaagacg gacuuugagn n 21 <210> SEQ ID NO 765 <211> LENGTH: 21 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interefering RNA - MKK7.4 <220> FEATURE: <221> NAME/KEY: misc_feature <222> LOCATION: 1, 2 <223> OTHER INFORMATION: n = A,T,C,G or U <400> SEQUENCE: 765 nncucaaagu ccgucuugca g 21 <210> SEQ ID NO 766 <211> LENGTH: 55 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Hairpin Vector - HP53-HP9 <400> SEQUENCE: 766 tttgactcca gtggtaatct acttcaagag agtagattac cactggagtc ttttt 55 <210> SEQ ID NO 767 <211> LENGTH: 55 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Hairpin Vector - HP53-HP9 <400> SEQUENCE: 767 ctagaaaaag actccagtgg taatctactc tcttgaagta gattaccact ggagt 55 <210> SEQ ID NO 768 <211> LENGTH: 55 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Hairpin Vector - HP53-HP9 <400> SEQUENCE: 768 uuugacucca gugguaaucu acuucaagag aguagauuac cacuggaguc uuuuu 55 <210> SEQ ID NO 769 <211> LENGTH: 55 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Hairpin Vector - HP53-HP9 <400> SEQUENCE: 769 cuagaaaaag acuccagugg uaaucuacuc ucuugaagua gauuaccacu ggagu 55 <210> SEQ ID NO 770 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interefering RNA - TCPTP1 <400> SEQUENCE: 770 aacagauaca gagauguaa 19 <210> SEQ ID NO 771 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interefering RNA - TCPTP1 <400> SEQUENCE: 771 uuacaucucu guaucuguu 19 <210> SEQ ID NO 772 <211> LENGTH: 21 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interefering RNA - TCPTP1 <220> FEATURE: <221> NAME/KEY: misc_feature <222> LOCATION: 20, 21 <223> OTHER INFORMATION: n = A,T,C,G or U <400> SEQUENCE: 772 aacagauaca gagauguaan n 21 <210> SEQ ID NO 773 <211> LENGTH: 21 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interefering RNA - TCPTP1 <220> FEATURE: <221> NAME/KEY: misc_feature <222> LOCATION: 1, 2 <223> OTHER INFORMATION: n = A,T,C,G or U <400> SEQUENCE: 773 nnuuacaucu cuguaucugu u 21 <210> SEQ ID NO 774 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interefering RNA - TCPTP2 <400> SEQUENCE: 774 aagcccauau gaucacagu 19 <210> SEQ ID NO 775 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interefering RNA - TCPTP2 <400> SEQUENCE: 775 acugugauca uaugggcuu 19 <210> SEQ ID NO 776 <211> LENGTH: 21 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interefering RNA - TCPTP2 <220> FEATURE: <221> NAME/KEY: misc_feature <222> LOCATION: 20, 21 <223> OTHER INFORMATION: n = A,T,C,G or U <400> SEQUENCE: 776 aagcccauau gaucacagun n 21 <210> SEQ ID NO 777 <211> LENGTH: 21 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interefering RNA - TCPTP2 <220> FEATURE: <221> NAME/KEY: misc_feature <222> LOCATION: 1, 2 <223> OTHER INFORMATION: n = A,T,C,G or U <400> SEQUENCE: 777 nnacugugau cauaugggcu u 21 <210> SEQ ID NO 778 <211> LENGTH: 926 <212> TYPE: DNA <213> ORGANISM: Homo sapiens <400> SEQUENCE: 778 ccccgccgct cctcctccct gtaacatgcc atagtgcgcc tgcgaccaca cggccggggc 60 gctagcgttc gccttcagcc accatgggga atgggatgaa caagatcctg cccggcctgt 120 acatcggcaa cttcaaagat gccagagacg cggaacaatt gagcaagaac aaggtgacac 180 atattctgtc tgtccacgat agtgccaggc ctatgttgga gggagttaaa tacctgtgca 240 tcccagcagc ggattcacca tctcaaaacc tgacaagaca tttcaaagaa agtattaaat 300 tcattcacga gtgccggctc cgcggtgaga gctgccttgt acactgcctg gccggggtct 360 ccaggagcgt gacactggtg atcgcataca tcatgaccgt cactgacttt ggctgggagg 420 atgccctgca caccgtgcgt gctgggagat cctgtgccaa ccccaacgtg ggcttccaga 480 gacagctcca ggagtttgag aagcatgagg tccatcagta tcggcagtgg ctgaaggaag 540 aatatggaga gagccctttg caggatgcag aagaagccaa aaacattctg gccgctccag 600 gaattctgaa gttctgggcc tttctcagaa gactgtaatg tacctgaagt ttctgaaata 660 ttgcaaaccc gcagagttta ggctggtgct gccaaaaaga aaagcaacat agagtttaag 720 tatccagtag tgatttgtaa acttgttttt catttgaagc tgaatatata cgtagtcatg 780 tttatgttga gaactaagga tattctttag caagagaaaa tattttcccc ttatccccac 840 tgctgtggag gtttctgtac ctcgcttgga tgcctgtaag gatcccggga gccttgccgc 900 actgccttgt gggtggcttg gcgctc 926 <210> SEQ ID NO 779 <211> LENGTH: 184 <212> TYPE: PRT <213> ORGANISM: Homo sapiens <400> SEQUENCE: 779 Met Gly Asn Gly Met Asn Lys Ile Leu Pro Gly Leu Tyr Ile Gly Asn 1 5 10 15 Phe Lys Asp Ala Arg Asp Ala Glu Gln Leu Ser Lys Asn Lys Val Thr 20 25 30 His Ile Leu Ser Val His Asp Ser Ala Arg Pro Met Leu Glu Gly Val 35 40 45 Lys Tyr Leu Cys Ile Pro Ala Ala Asp Ser Pro Ser Gln Asn Leu Thr 50 55 60 Arg His Phe Lys Glu Ser Ile Lys Phe Ile His Glu Cys Arg Leu Arg 65 70 75 80 Gly Glu Ser Cys Leu Val His Cys Leu Ala Gly Val Ser Arg Ser Val 85 90 95 Thr Leu Val Ile Ala Tyr Ile Met Thr Val Thr Asp Phe Gly Trp Glu 100 105 110 Asp Ala Leu His Thr Val Arg Ala Gly Arg Ser Cys Ala Asn Pro Asn 115 120 125 Val Gly Phe Gln Arg Gln Leu Gln Glu Phe Glu Lys His Glu Val His 130 135 140 Gln Tyr Arg Gln Trp Leu Lys Glu Glu Tyr Gly Glu Ser Pro Leu Gln 145 150 155 160 Asp Ala Glu Glu Ala Lys Asn Ile Leu Ala Ala Pro Gly Ile Leu Lys 165 170 175 Phe Trp Ala Phe Leu Arg Arg Leu 180 <210> SEQ ID NO 780 <211> LENGTH: 707 <212> TYPE: DNA <213> ORGANISM: Homo sapiens <400> SEQUENCE: 780 tgacccgctg tcctgtgccc tttcccagcg atgggcgtgc agccccccaa cttctcctgg 60 gtgcttccgg gccggctggc gggactggcg ctgccgcggc tccccgccca ctaccagttc 120 ctgttggacc tgggcgtgcg gcacctggtg tccctgacgg agcgcgggcc ccctcacagc 180 gacagctgcc ccggcctcac cctgcaccgc ctgcgcatcc ccgacttctg cccgccggcc 240 cccgaccaga tcgaccgctt cgtgcagatc gtggacgagg ccaacgcacg gggagaggct 300 gtgggagtgc actgtgctct gggctttggc cgcactggca ccatgctggc ctgttacctg 360 gtgaaggagc ggggcttggc tgcaggagat gccattgctg aaatccgacg actacgaccc 420 ggctccatcg agacctatga gcaggagaaa gcagtcttcc agttctacca gcgaacgaaa 480 taaggggcct tagtaccctt ctaccaggcc ctcactcccc ttccccatgt tgtcgatggg 540 gccagagatg aagggaagtg gactaaagta ttaaaccctc tagctcccat tggctgaaga 600 cactgaagta gcccacccct gcaggcaggt cctgattgaa ggggaggctt gtactgcttt 660 gttgaataaa tgagttttac gaaccaaaaa aaaaaaaaaa aaaaaaa 707 <210> SEQ ID NO 781 <211> LENGTH: 150 <212> TYPE: PRT <213> ORGANISM: Homo sapiens <400> SEQUENCE: 781 Met Gly Val Gln Pro Pro Asn Phe Ser Trp Val Leu Pro Gly Arg Leu 1 5 10 15 Ala Gly Leu Ala Leu Pro Arg Leu Pro Ala His Tyr Gln Phe Leu Leu 20 25 30 Asp Leu Gly Val Arg His Leu Val Ser Leu Thr Glu Arg Gly Pro Pro 35 40 45 His Ser Asp Ser Cys Pro Gly Leu Thr Leu His Arg Leu Arg Ile Pro 50 55 60 Asp Phe Cys Pro Pro Ala Pro Asp Gln Ile Asp Arg Phe Val Gln Ile 65 70 75 80 Val Asp Glu Ala Asn Ala Arg Gly Glu Ala Val Gly Val His Cys Ala 85 90 95 Leu Gly Phe Gly Arg Thr Gly Thr Met Leu Ala Cys Tyr Leu Val Lys 100 105 110 Glu Arg Gly Leu Ala Ala Gly Asp Ala Ile Ala Glu Ile Arg Arg Leu 115 120 125 Arg Pro Gly Ser Ile Glu Thr Tyr Glu Gln Glu Lys Ala Val Phe Gln 130 135 140 Phe Tyr Gln Arg Thr Lys 145 150 <210> SEQ ID NO 782 <211> LENGTH: 833 <212> TYPE: DNA <213> ORGANISM: Homo sapiens <400> SEQUENCE: 782 ggccccccgt tccccgccag gctgcaggcg tcgggcctgg gccgtcaggg cagctgtgac 60 cggatcgctt cccgggcggc gagctggggg tgcacccgga ccgccgcccc cgggatcatg 120 ggcaatggca tgaccaaggt acttcctgga ctctacctcg gaaacttcat tgatgccaaa 180 gacctggatc agctgggccg aaataagatc acacacatca tctctatcca tgagtcaccc 240 cagcctctgc tgcaggatat cacctacctt cgcatcccgg tcgctgatac ccctgaggta 300 cccatcaaaa agcacttcaa agaatgtatc aacttcatcc actgctgccg ccttaatggg 360 gggaactgcc ttgtgcactg ctttgcaggc atctctcgca gcaccacgat tgtgacagcg 420 tatgtgatga ctgtgacggg gctaggctgg cgggacgtgc ttgaagccat caaggccacc 480 aggcccatcg ccaaccccaa cccaggcttt aggcagcagc ttgaagagtt tggctgggcc 540 agttcccaga agcttcgccg gcagctggag gagcgcttcg gcgagagccc cttccgcgac 600 gaggaggagt tgcgcgcgct gctgccgctg tgcaagcgct gccggcaggg ctccgcgacc 660 tcggcctcct ccgccgggcc gcactcagca gcctccgagg gaaccgtgca gcgcctggtg 720 ccgcgcacgc cccgggaagc ccaccggccg ctgccgctgc tggcgcgcgt caagcagact 780 ttctcttgcc tcccccggtg tctgtcccgc aagggcggca agtgaggatg cag 833 <210> SEQ ID NO 783 <211> LENGTH: 235 <212> TYPE: PRT <213> ORGANISM: Homo sapiens <400> SEQUENCE: 783 Met Gly Asn Gly Met Thr Lys Val Leu Pro Gly Leu Tyr Leu Gly Asn 1 5 10 15 Phe Ile Asp Ala Lys Asp Leu Asp Gln Leu Gly Arg Asn Lys Ile Thr 20 25 30 His Ile Ile Ser Ile His Glu Ser Pro Gln Pro Leu Leu Gln Asp Ile 35 40 45 Thr Tyr Leu Arg Ile Pro Val Ala Asp Thr Pro Glu Val Pro Ile Lys 50 55 60 Lys His Phe Lys Glu Cys Ile Asn Phe Ile His Cys Cys Arg Leu Asn 65 70 75 80 Gly Gly Asn Cys Leu Val His Cys Phe Ala Gly Ile Ser Arg Ser Thr 85 90 95 Thr Ile Val Thr Ala Tyr Val Met Thr Val Thr Gly Leu Gly Trp Arg 100 105 110 Asp Val Leu Glu Ala Ile Lys Ala Thr Arg Pro Ile Ala Asn Pro Asn 115 120 125 Pro Gly Phe Arg Gln Gln Leu Glu Glu Phe Gly Trp Ala Ser Ser Gln 130 135 140 Lys Leu Arg Arg Gln Leu Glu Glu Arg Phe Gly Glu Ser Pro Phe Arg 145 150 155 160 Asp Glu Glu Glu Leu Arg Ala Leu Leu Pro Leu Cys Lys Arg Cys Arg 165 170 175 Gln Gly Ser Ala Thr Ser Ala Ser Ser Ala Gly Pro His Ser Ala Ala 180 185 190 Ser Glu Gly Thr Val Gln Arg Leu Val Pro Arg Thr Pro Arg Glu Ala 195 200 205 His Arg Pro Leu Pro Leu Leu Ala Arg Val Lys Gln Thr Phe Ser Cys 210 215 220 Leu Pro Arg Cys Leu Ser Arg Lys Gly Gly Lys 225 230 235 <210> SEQ ID NO 784 <211> LENGTH: 1711 <212> TYPE: DNA <213> ORGANISM: Homo sapiens <400> SEQUENCE: 784 cctgggaaga agttatctat ctctcgagtg acattcaaga tataccgtac ccctcggttc 60 tgtaagtcct ctaagttgga ggcattccat tctgagccgg ccccatgacc ctgagcacgt 120 tggcccgcaa gaggaaggcg cccctcgctt gcacctgcag cctcggtggc cccgacatga 180 ttccttactt ctccgccaac gcggtcatct cgcagaacgc catcaaccag ctcatcagcg 240 agagctttct aactgtcaaa ggtgctgccc tttttctacc acggggaaat ggctcatcca 300 caccaagaat cagccacaga cggaacaagc atgcaggcga tctccaacag catctccaag 360 caatgttcat tttactccgc ccagaagaca acatcaggct ggctgtaaga ctggaaagta 420 cttaccagaa tcgaacacgc tatatggtag tggtttcaac taatggtaga caagacactg 480 aagaaagcat cgtcctagga atggatttct cctctaatga cagtagcact tgtaccatgg 540 gcttagtttt gcctctctgg agcgacacgc taattcattt ggatggtgat ggtgggttca 600 gtgtatcgac ggataacaga gttcacatat tcaaacctgt atctgtgcag gcaatgtggt 660 ctgcactaca gagcttacac aaggcttgtg aagtcgccag agcgcataac tactacccag 720 gcagcctatt tctcacttgg gtgagttatt atgagagcca tatcaactca gatcaatcct 780 cagtcaatga atggaatgca atgcaagatg tacagtccca ccggcccgac tctccagctc 840 tcttcaccga catacctact gaacgtgaac gaacagaaag gctaattaaa accaaattaa 900 gggagatcat gatgcagaag gatttggaga atattacatc caaagagata agaacagagt 960 tggaaatgca aatggtgtgc aacttgcggg aattcaagga atttatagac aatgaaatga 1020 tagtgatcct tggtcaaatg gatagcccta cacagatatt tgagcatgtg ttcctgggct 1080 cagaatggaa tgcctccaac ttagaggact tacagaaccg aggggtacgg tatatcttga 1140 atgtcactcg agagatagat aacttcttcc caggagtctt tgagtatcat aacattcggg 1200 tatatgatga agaggcaacg gatctcctgg cgtactggaa tgacacttac aaattcatct 1260 ctaaagcaaa gaaacatgga tctaaatgcc ttgtgcactg caaaatgggg gtgagtcgct 1320 cagcctccac cgtgattgcc tatgcaatga aggaatatgg ctggaatctg gaccgagcct 1380 atgactatgt gaaagaaaga cgaacggtaa ccaagcccaa cccaagcttc atgagacaac 1440 tggaagagta tcaggggatc ttgctggcaa gcttcctagg cttgattcat ggagggaggg 1500 acaagccctg gggagagaaa agcacagaat ttgagtcagt agatctggtt tccattcctg 1560 gttcaccctc ttgctgcaac cctgagaagt tacttcacat ttctcatcct tacctgaccc 1620 catctataaa atgaaaatca agagatccat ctcacagggt tattgtgaat aaaaatgtgt 1680 ttgaatgttt ataaaaaaaa aaaaaaaaaa a 1711 <210> SEQ ID NO 785 <211> LENGTH: 509 <212> TYPE: PRT <213> ORGANISM: Homo sapiens <400> SEQUENCE: 785 Met Thr Leu Ser Thr Leu Ala Arg Lys Arg Lys Ala Pro Leu Ala Cys 1 5 10 15 Thr Cys Ser Leu Gly Gly Pro Asp Met Ile Pro Tyr Phe Ser Ala Asn 20 25 30 Ala Val Ile Ser Gln Asn Ala Ile Asn Gln Leu Ile Ser Glu Ser Phe 35 40 45 Leu Thr Val Lys Gly Ala Ala Leu Phe Leu Pro Arg Gly Asn Gly Ser 50 55 60 Ser Thr Pro Arg Ile Ser His Arg Arg Asn Lys His Ala Gly Asp Leu 65 70 75 80 Gln Gln His Leu Gln Ala Met Phe Ile Leu Leu Arg Pro Glu Asp Asn 85 90 95 Ile Arg Leu Ala Val Arg Leu Glu Ser Thr Tyr Gln Asn Arg Thr Arg 100 105 110 Tyr Met Val Val Val Ser Thr Asn Gly Arg Gln Asp Thr Glu Glu Ser 115 120 125 Ile Val Leu Gly Met Asp Phe Ser Ser Asn Asp Ser Ser Thr Cys Thr 130 135 140 Met Gly Leu Val Leu Pro Leu Trp Ser Asp Thr Leu Ile His Leu Asp 145 150 155 160 Gly Asp Gly Gly Phe Ser Val Ser Thr Asp Asn Arg Val His Ile Phe 165 170 175 Lys Pro Val Ser Val Gln Ala Met Trp Ser Ala Leu Gln Ser Leu His 180 185 190 Lys Ala Cys Glu Val Ala Arg Ala His Asn Tyr Tyr Pro Gly Ser Leu 195 200 205 Phe Leu Thr Trp Val Ser Tyr Tyr Glu Ser His Ile Asn Ser Asp Gln 210 215 220 Ser Ser Val Asn Glu Trp Asn Ala Met Gln Asp Val Gln Ser His Arg 225 230 235 240 Pro Asp Ser Pro Ala Leu Phe Thr Asp Ile Pro Thr Glu Arg Glu Arg 245 250 255 Thr Glu Arg Leu Ile Lys Thr Lys Leu Arg Glu Ile Met Met Gln Lys 260 265 270 Asp Leu Glu Asn Ile Thr Ser Lys Glu Ile Arg Thr Glu Leu Glu Met 275 280 285 Gln Met Val Cys Asn Leu Arg Glu Phe Lys Glu Phe Ile Asp Asn Glu 290 295 300 Met Ile Val Ile Leu Gly Gln Met Asp Ser Pro Thr Gln Ile Phe Glu 305 310 315 320 His Val Phe Leu Gly Ser Glu Trp Asn Ala Ser Asn Leu Glu Asp Leu 325 330 335 Gln Asn Arg Gly Val Arg Tyr Ile Leu Asn Val Thr Arg Glu Ile Asp 340 345 350 Asn Phe Phe Pro Gly Val Phe Glu Tyr His Asn Ile Arg Val Tyr Asp 355 360 365 Glu Glu Ala Thr Asp Leu Leu Ala Tyr Trp Asn Asp Thr Tyr Lys Phe 370 375 380 Ile Ser Lys Ala Lys Lys His Gly Ser Lys Cys Leu Val His Cys Lys 385 390 395 400 Met Gly Val Ser Arg Ser Ala Ser Thr Val Ile Ala Tyr Ala Met Lys 405 410 415 Glu Tyr Gly Trp Asn Leu Asp Arg Ala Tyr Asp Tyr Val Lys Glu Arg 420 425 430 Arg Thr Val Thr Lys Pro Asn Pro Ser Phe Met Arg Gln Leu Glu Glu 435 440 445 Tyr Gln Gly Ile Leu Leu Ala Ser Phe Leu Gly Leu Ile His Gly Gly 450 455 460 Arg Asp Lys Pro Trp Gly Glu Lys Ser Thr Glu Phe Glu Ser Val Asp 465 470 475 480 Leu Val Ser Ile Pro Gly Ser Pro Ser Cys Cys Asn Pro Glu Lys Leu 485 490 495 Leu His Ile Ser His Pro Tyr Leu Thr Pro Ser Ile Lys 500 505 <210> SEQ ID NO 786 <211> LENGTH: 1165 <212> TYPE: DNA <213> ORGANISM: Homo sapiens <400> SEQUENCE: 786 ggccagtggg ggtggctggg cgtgcggctg ctacatgccc cacggaccag aacctcccga 60 cgcggccagg ccccggcaca cccagctgca gaaaggagag aaaatccctt ggctctaaaa 120 tgacatctgg agaagtgaag acaagcctca agaatgccta ctcatctgcc aagaggctgt 180 cgccgaagat ggaggaggaa ggggaggagg aggactactg cacccctgga gcctttgagc 240 tggagcggct cttctggaag ggcagtcccc agtacaccca cgtcaacgag gtctggccca 300 agctctacat tggcgatgag gcgacggcgc tggaccgcta taggctgcag aaggcggggt 360 tcacgcacgt gctgaacgcg gcccacggcc gctggaacgt ggacactggg cccgactact 420 accgcgacat ggacatccag taccacggcg tggaggccga cgacctgccc accttcgacc 480 tcagtgtctt cttctacccg gcggcagcct tcatcgacag agcgctaagc gacgaccaca 540 gtaagatcct ggttcactgc gtcatgggcc gcagccggtc agccaccctg gtcctggcct 600 acctgatgat ccacaaggac atgaccctgg tggacgccat ccagcaagtg gccaagaacc 660 gctgcgtcct cccgaaccgg ggctttttga agcagctccg ggagctggac aagcagctgg 720 tgcagcagag gcgacggtcc cagcgccagg acggtgagga ggaggatggc agggagctgt 780 aggcccgact cacagggcca gcagaggcac ttggggacag aggggagagg cagaacatag 840 ccctggccta ggactccaga gaagggatgg tgaaaccgaa gctcgactct tccaaaccat 900 cttgttcaac ttccccatgt gtgctgggga cagggaggac ccagagctgc ccccgggcag 960 agctgagcgc tcagcctctc agcaaaatgg gagggacggg ctccccggct ctgggtcaca 1020 gaggagcatg ccacgctgca ccaagtctcc tgctttggtt ttgttttttt ggtgagaagg 1080 aagagggaaa aagattttta aaatgtgtag gcagtatgtt gtgattaaac gtttggcttt 1140 gtccaaaaaa aaaaaaaaaa aaaaa 1165 <210> SEQ ID NO 787 <211> LENGTH: 220 <212> TYPE: PRT <213> ORGANISM: Homo sapiens <400> SEQUENCE: 787 Met Thr Ser Gly Glu Val Lys Thr Ser Leu Lys Asn Ala Tyr Ser Ser 1 5 10 15 Ala Lys Arg Leu Ser Pro Lys Met Glu Glu Glu Gly Glu Glu Glu Asp 20 25 30 Tyr Cys Thr Pro Gly Ala Phe Glu Leu Glu Arg Leu Phe Trp Lys Gly 35 40 45 Ser Pro Gln Tyr Thr His Val Asn Glu Val Trp Pro Lys Leu Tyr Ile 50 55 60 Gly Asp Glu Ala Thr Ala Leu Asp Arg Tyr Arg Leu Gln Lys Ala Gly 65 70 75 80 Phe Thr His Val Leu Asn Ala Ala His Gly Arg Trp Asn Val Asp Thr 85 90 95 Gly Pro Asp Tyr Tyr Arg Asp Met Asp Ile Gln Tyr His Gly Val Glu 100 105 110 Ala Asp Asp Leu Pro Thr Phe Asp Leu Ser Val Phe Phe Tyr Pro Ala 115 120 125 Ala Ala Phe Ile Asp Arg Ala Leu Ser Asp Asp His Ser Lys Ile Leu 130 135 140 Val His Cys Val Met Gly Arg Ser Arg Ser Ala Thr Leu Val Leu Ala 145 150 155 160 Tyr Leu Met Ile His Lys Asp Met Thr Leu Val Asp Ala Ile Gln Gln 165 170 175 Val Ala Lys Asn Arg Cys Val Leu Pro Asn Arg Gly Phe Leu Lys Gln 180 185 190 Leu Arg Glu Leu Asp Lys Gln Leu Val Gln Gln Arg Arg Arg Ser Gln 195 200 205 Arg Gln Asp Gly Glu Glu Glu Asp Gly Arg Glu Leu 210 215 220 <210> SEQ ID NO 788 <211> LENGTH: 2276 <212> TYPE: DNA <213> ORGANISM: Homo sapiens <400> SEQUENCE: 788 ctgccccgcg tccggtcccg agcgggcctc cctcgggcca gcccgatgtg accgagccca 60 gcggagcctg agcaaggagc gggtccgtcg cggagccgga gggcgggagg aacatgacat 120 cgcggagatg gtttcaccca aatatcactg gtgtggaggc agaaaaccta ctgttgacaa 180 gaggagttga tggcagtttt ttggcaaggc ctagtaaaag taaccctgga gacttcacac 240 tttccgttag aagaaatgga gctgtcaccc acatcaagat tcagaacact ggtgattact 300 atgacctgta tggaggggag aaatttgcca ctttggctga gttggtccag tattacatgg 360 aacatcacgg gcaattaaaa gagaagaatg gagatgtcat tgagcttaaa tatcctctga 420 actgtgcaga tcctacctct gaaaggtggt ttcatggaca tctctctggg aaagaagcag 480 agaaattatt aactgaaaaa ggaaaacatg gtagttttct tgtacgagag agccagagcc 540 accctggaga ttttgttctt tctgtgcgca ctggtgatga caaaggggag agcaatgacg 600 gcaagtctaa agtgacccat gttatgattc gctgtcagga actgaaatac gacgttggtg 660 gaggagaacg gtttgattct ttgacagatc ttgtggaaca ttataagaag aatcctatgg 720 tggaaacatt gggtacagta ctacaactca agcagcccct taacacgact cgtataaatg 780 ctgctgaaat agaaagcaga gttcgagaac taagcaaatt agctgagacc acagataaag 840 tcaaacaagg cttttgggaa gaatttgaga cactacaaca acaggagtgc aaacttctct 900 acagccgaaa agagggtcaa aggcaagaaa acaaaaacaa aaatagatat aaaaacatcc 960 tgccctttga tcataccagg gttgtcctac acgatggtga tcccaatgag cctgtttcag 1020 attacatcaa tgcaaatatc atcatgcctg aatttgaaac caagtgcaac aattcaaagc 1080 ccaaaaagag ttacattgcc acacaaggct gcctgcaaaa cacggtgaat gacttttggc 1140 ggatggtgtt ccaagaaaac tcccgagtga ttgtcatgac aacgaaagaa gtggagagag 1200 gaaagagtaa atgtgtcaaa tactggcctg atgagtatgc tctaaaagaa tatggcgtca 1260 tgcgtgttag gaacgtcaaa gaaagcgccg ctcatgacta tacgctaaga gaacttaaac 1320 tttcaaaggt tggacaaggg aatacggaga gaacggtctg gcaataccac tttcggacct 1380 ggccggacca cggcgtgccc agcgaccctg ggggcgtgct ggacttcctg gaggaggtgc 1440 accataagca ggagagcatc atggatgcag ggccggtcgt ggtgcactgc agtgctggaa 1500 ttggccggac agggacgttc attgtgattg atattcttat tgacatcatc agagagaaag 1560 gtgttgactg cgatattgac gttcccaaaa ccatccagat ggtgcggtct cagaggtcag 1620 ggatggtcca gacagaagca cagtaccgat ttatctatat ggcggtccag cattatattg 1680 aaacactaca gcgcaggatt gaagaagagc agaaaagcaa gaggaaaggg cacgaatata 1740 caaatattaa gtattctcta gcggaccaga cgagtggaga tcagagccct ctcccgcctt 1800 gtactccaac gccaccctgt gcagaaatga gagaagacag tgctagagtc tatgaaaacg 1860 tgggcctgat gcaacagcag aaaagtttca gatgagaaaa cctgccaaaa cttcagcaca 1920 gaaatagatg tggactttca ccctctccct aaaaagatca agaacagacg caagaaagtt 1980 tatgtgaaga cagaatttgg atttggaagg cttgcaatgt ggttgactac cttttgataa 2040 gcaaaatttg aaaccattta aagaccactg tattttaact caacaatacc tgcttcccaa 2100 ttactcattt cctcagataa gaagaaatca tctctacaat gtagacaaca ttatatttta 2160 tagaatttgt ttgaaattga ggaagcagtt aaattgtgcg ctgtattttg cagattatgg 2220 ggattcaaat tctagtaata ggctttttta tttttatttt tataccctta accagg 2276 <210> SEQ ID NO 789 <211> LENGTH: 593 <212> TYPE: PRT <213> ORGANISM: Homo sapiens <400> SEQUENCE: 789 Met Thr Ser Arg Arg Trp Phe His Pro Asn Ile Thr Gly Val Glu Ala 1 5 10 15 Glu Asn Leu Leu Leu Thr Arg Gly Val Asp Gly Ser Phe Leu Ala Arg 20 25 30 Pro Ser Lys Ser Asn Pro Gly Asp Phe Thr Leu Ser Val Arg Arg Asn 35 40 45 Gly Ala Val Thr His Ile Lys Ile Gln Asn Thr Gly Asp Tyr Tyr Asp 50 55 60 Leu Tyr Gly Gly Glu Lys Phe Ala Thr Leu Ala Glu Leu Val Gln Tyr 65 70 75 80 Tyr Met Glu His His Gly Gln Leu Lys Glu Lys Asn Gly Asp Val Ile 85 90 95 Glu Leu Lys Tyr Pro Leu Asn Cys Ala Asp Pro Thr Ser Glu Arg Trp 100 105 110 Phe His Gly His Leu Ser Gly Lys Glu Ala Glu Lys Leu Leu Thr Glu 115 120 125 Lys Gly Lys His Gly Ser Phe Leu Val Arg Glu Ser Gln Ser His Pro 130 135 140 Gly Asp Phe Val Leu Ser Val Arg Thr Gly Asp Asp Lys Gly Glu Ser 145 150 155 160 Asn Asp Gly Lys Ser Lys Val Thr His Val Met Ile Arg Cys Gln Glu 165 170 175 Leu Lys Tyr Asp Val Gly Gly Gly Glu Arg Phe Asp Ser Leu Thr Asp 180 185 190 Leu Val Glu His Tyr Lys Lys Asn Pro Met Val Glu Thr Leu Gly Thr 195 200 205 Val Leu Gln Leu Lys Gln Pro Leu Asn Thr Thr Arg Ile Asn Ala Ala 210 215 220 Glu Ile Glu Ser Arg Val Arg Glu Leu Ser Lys Leu Ala Glu Thr Thr 225 230 235 240 Asp Lys Val Lys Gln Gly Phe Trp Glu Glu Phe Glu Thr Leu Gln Gln 245 250 255 Gln Glu Cys Lys Leu Leu Tyr Ser Arg Lys Glu Gly Gln Arg Gln Glu 260 265 270 Asn Lys Asn Lys Asn Arg Tyr Lys Asn Ile Leu Pro Phe Asp His Thr 275 280 285 Arg Val Val Leu His Asp Gly Asp Pro Asn Glu Pro Val Ser Asp Tyr 290 295 300 Ile Asn Ala Asn Ile Ile Met Pro Glu Phe Glu Thr Lys Cys Asn Asn 305 310 315 320 Ser Lys Pro Lys Lys Ser Tyr Ile Ala Thr Gln Gly Cys Leu Gln Asn 325 330 335 Thr Val Asn Asp Phe Trp Arg Met Val Phe Gln Glu Asn Ser Arg Val 340 345 350 Ile Val Met Thr Thr Lys Glu Val Glu Arg Gly Lys Ser Lys Cys Val 355 360 365 Lys Tyr Trp Pro Asp Glu Tyr Ala Leu Lys Glu Tyr Gly Val Met Arg 370 375 380 Val Arg Asn Val Lys Glu Ser Ala Ala His Asp Tyr Thr Leu Arg Glu 385 390 395 400 Leu Lys Leu Ser Lys Val Gly Gln Gly Asn Thr Glu Arg Thr Val Trp 405 410 415 Gln Tyr His Phe Arg Thr Trp Pro Asp His Gly Val Pro Ser Asp Pro 420 425 430 Gly Gly Val Leu Asp Phe Leu Glu Glu Val His His Lys Gln Glu Ser 435 440 445 Ile Met Asp Ala Gly Pro Val Val Val His Cys Ser Ala Gly Ile Gly 450 455 460 Arg Thr Gly Thr Phe Ile Val Ile Asp Ile Leu Ile Asp Ile Ile Arg 465 470 475 480 Glu Lys Gly Val Asp Cys Asp Ile Asp Val Pro Lys Thr Ile Gln Met 485 490 495 Val Arg Ser Gln Arg Ser Gly Met Val Gln Thr Glu Ala Gln Tyr Arg 500 505 510 Phe Ile Tyr Met Ala Val Gln His Tyr Ile Glu Thr Leu Gln Arg Arg 515 520 525 Ile Glu Glu Glu Gln Lys Ser Lys Arg Lys Gly His Glu Tyr Thr Asn 530 535 540 Ile Lys Tyr Ser Leu Ala Asp Gln Thr Ser Gly Asp Gln Ser Pro Leu 545 550 555 560 Pro Pro Cys Thr Pro Thr Pro Pro Cys Ala Glu Met Arg Glu Asp Ser 565 570 575 Ala Arg Val Tyr Glu Asn Val Gly Leu Met Gln Gln Gln Lys Ser Phe 580 585 590 Arg <210> SEQ ID NO 790 <211> LENGTH: 2121 <212> TYPE: DNA <213> ORGANISM: Homo sapiens <400> SEQUENCE: 790 cgccaggcct ggaggggggt ctgtgcgcgg ccggctggct ctgccccgcg tccggtcccg 60 agcgggcctc cctcgggcca gcccgatgtg accgagccca gcggagcctg agcaaggagc 120 gggtccgtcg cggagccgga gggcgggagg aacatgacat cgcggagatg gtttcaccca 180 aatatcactg gtgtggaggc agaaaaccta ctgttgacaa gaggagttga tggcagtttt 240 ttggcaaggc ctagtaaaag taaccctgga gacttcacac tttccgttag aagaaatgga 300 gctgtcaccc acatcaagat tcagaacact ggtgattact atgacctgta tggaggggag 360 aaatttgcca ctttggctga gttggtccag tattacatgg aacatcacgg gcaattaaaa 420 gagaagaatg gagatgtcat tgagcttaaa tatcctctga actgtgcaga tcctacctct 480 gaaaggtggt ttcatggaca tctctctggg aaagaagcag agaaattatt aactgaaaaa 540 ggaaaacatg gtagttttct tgtacgagag agccagagcc accctggaga ttttgttctt 600 tctgtgcgca ctggtgatga caaaggggag agcaatgacg gcaagtctaa agtgacccat 660 gttatgattc gctgtcagga actgaaatac gacgttggtg gaggagaacg gtttgattct 720 ttgacagatc ttgtggaaca ttataagaag aatcctatgg tggaaacatt gggtacagta 780 ctacaactca agcagcccct taacacgact cgtataaatg ctgctgaaat agaaagcaga 840 gttcgagaac taagcaaatt agctgagacc acagataaag tcaaacaagg cttttgggaa 900 gaatttgaga cactacaaca acaggagtgc aaacttctct acagccgaaa agagggtcaa 960 aggcaagaaa acaaaaacaa aaatagatat aaaaacatcc tgccctttga tcataccagg 1020 gttgtcctac acgatggtga tcccaatgag cctgtttcag attacatcaa tgcaaatatc 1080 atcatgcctg aatttgaaac caagtgcaac aattcaaagc ccaaaaagag ttacattgcc 1140 acacaaggct gcctgcaaaa cacggtgaat gacttttggc ggatggtgtt ccaagaaaac 1200 tcccgagtga ttgtcatgac aacgaaagaa gtggagagag gaaagagtaa atgtgtcaaa 1260 tactggcctg atgagtatgc tctaaaagaa tatggcgtca tgcgtgttag gaacgtcaaa 1320 gaaagcgccg ctcatgacta tacgctaaga gaacttaaac tttcaaaggt tggacaaggg 1380 aatacggaga gaacggtctg gcaataccac tttcggacct ggccggacca cggcgtgccc 1440 agcgaccctg ggggcgtgct ggacttcctg gaggaggtgc accataagca ggagagcatc 1500 atggatgcag ggccggtcgt ggtgcactgc agtgctggaa ttggccggac agggacgttc 1560 attgtgattg atattcttat tgacatcatc agagagaaag gtgttgactg cgatattgac 1620 gttcccaaaa ccatccagat ggtgcggtct cagaggtcag ggatggtcca gacagaagca 1680 cagtaccgat ttatctatat ggcggtccag cattatattg aaacactaca gcgcaggatt 1740 gaagaagagc agaaaagcaa gaggaaaggg cacgaatata caaatattaa gtattctcta 1800 gcggaccaga cgagtggaga tcagagccct ctcccgcctt gtactccaac gccaccctgt 1860 gcagaaatga gagaagacag tgctagagtc tatgaaaacg tgggcctgat gcaacagcag 1920 aaaagtttca gatgagaaaa cctgccaaaa cttcagcaca gaaatagatg tggactttca 1980 ccctctccct aaaaagatca agaacagacg caagaaagtt tatgtgaaga cagaatttgg 2040 atttggaagg cttgcaatgt ggttgactac cttttgataa gcaaaatttg aaaccattta 2100 aagaccactg tattttaact c 2121 <210> SEQ ID NO 791 <211> LENGTH: 593 <212> TYPE: PRT <213> ORGANISM: Homo sapiens <400> SEQUENCE: 791 Met Thr Ser Arg Arg Trp Phe His Pro Asn Ile Thr Gly Val Glu Ala 1 5 10 15 Glu Asn Leu Leu Leu Thr Arg Gly Val Asp Gly Ser Phe Leu Ala Arg 20 25 30 Pro Ser Lys Ser Asn Pro Gly Asp Phe Thr Leu Ser Val Arg Arg Asn 35 40 45 Gly Ala Val Thr His Ile Lys Ile Gln Asn Thr Gly Asp Tyr Tyr Asp 50 55 60 Leu Tyr Gly Gly Glu Lys Phe Ala Thr Leu Ala Glu Leu Val Gln Tyr 65 70 75 80 Tyr Met Glu His His Gly Gln Leu Lys Glu Lys Asn Gly Asp Val Ile 85 90 95 Glu Leu Lys Tyr Pro Leu Asn Cys Ala Asp Pro Thr Ser Glu Arg Trp 100 105 110 Phe His Gly His Leu Ser Gly Lys Glu Ala Glu Lys Leu Leu Thr Glu 115 120 125 Lys Gly Lys His Gly Ser Phe Leu Val Arg Glu Ser Gln Ser His Pro 130 135 140 Gly Asp Phe Val Leu Ser Val Arg Thr Gly Asp Asp Lys Gly Glu Ser 145 150 155 160 Asn Asp Gly Lys Ser Lys Val Thr His Val Met Ile Arg Cys Gln Glu 165 170 175 Leu Lys Tyr Asp Val Gly Gly Gly Glu Arg Phe Asp Ser Leu Thr Asp 180 185 190 Leu Val Glu His Tyr Lys Lys Asn Pro Met Val Glu Thr Leu Gly Thr 195 200 205 Val Leu Gln Leu Lys Gln Pro Leu Asn Thr Thr Arg Ile Asn Ala Ala 210 215 220 Glu Ile Glu Ser Arg Val Arg Glu Leu Ser Lys Leu Ala Glu Thr Thr 225 230 235 240 Asp Lys Val Lys Gln Gly Phe Trp Glu Glu Phe Glu Thr Leu Gln Gln 245 250 255 Gln Glu Cys Lys Leu Leu Tyr Ser Arg Lys Glu Gly Gln Arg Gln Glu 260 265 270 Asn Lys Asn Lys Asn Arg Tyr Lys Asn Ile Leu Pro Phe Asp His Thr 275 280 285 Arg Val Val Leu His Asp Gly Asp Pro Asn Glu Pro Val Ser Asp Tyr 290 295 300 Ile Asn Ala Asn Ile Ile Met Pro Glu Phe Glu Thr Lys Cys Asn Asn 305 310 315 320 Ser Lys Pro Lys Lys Ser Tyr Ile Ala Thr Gln Gly Cys Leu Gln Asn 325 330 335 Thr Val Asn Asp Phe Trp Arg Met Val Phe Gln Glu Asn Ser Arg Val 340 345 350 Ile Val Met Thr Thr Lys Glu Val Glu Arg Gly Lys Ser Lys Cys Val 355 360 365 Lys Tyr Trp Pro Asp Glu Tyr Ala Leu Lys Glu Tyr Gly Val Met Arg 370 375 380 Val Arg Asn Val Lys Glu Ser Ala Ala His Asp Tyr Thr Leu Arg Glu 385 390 395 400 Leu Lys Leu Ser Lys Val Gly Gln Gly Asn Thr Glu Arg Thr Val Trp 405 410 415 Gln Tyr His Phe Arg Thr Trp Pro Asp His Gly Val Pro Ser Asp Pro 420 425 430 Gly Gly Val Leu Asp Phe Leu Glu Glu Val His His Lys Gln Glu Ser 435 440 445 Ile Met Asp Ala Gly Pro Val Val Val His Cys Ser Ala Gly Ile Gly 450 455 460 Arg Thr Gly Thr Phe Ile Val Ile Asp Ile Leu Ile Asp Ile Ile Arg 465 470 475 480 Glu Lys Gly Val Asp Cys Asp Ile Asp Val Pro Lys Thr Ile Gln Met 485 490 495 Val Arg Ser Gln Arg Ser Gly Met Val Gln Thr Glu Ala Gln Tyr Arg 500 505 510 Phe Ile Tyr Met Ala Val Gln His Tyr Ile Glu Thr Leu Gln Arg Arg 515 520 525 Ile Glu Glu Glu Gln Lys Ser Lys Arg Lys Gly His Glu Tyr Thr Asn 530 535 540 Ile Lys Tyr Ser Leu Ala Asp Gln Thr Ser Gly Asp Gln Ser Pro Leu 545 550 555 560 Pro Pro Cys Thr Pro Thr Pro Pro Cys Ala Glu Met Arg Glu Asp Ser 565 570 575 Ala Arg Val Tyr Glu Asn Val Gly Leu Met Gln Gln Gln Lys Ser Phe 580 585 590 Arg <210> SEQ ID NO 792 <211> LENGTH: 2654 <212> TYPE: DNA <213> ORGANISM: Homo sapiens <400> SEQUENCE: 792 agccggagct ggagccgagg cggcggcggg acgcggccgg ccggacaaat ttcctgctag 60 gctgcggacg agcgggcggc aggagccggc gcgagcggct tcaggaaccc acggcctctg 120 cgcgtccccg cgacccttct tcgcgcccgg cgaagacagc cgggcgcccc ggagggcggc 180 gggcaggcgc ccgggagatg cggagcctcc gctgcagcgc gatctgcgcg accagaccgg 240 cccccccgag actatagcct tcactttccc tcggtccacc atggagccct tgtgtccact 300 cctgctggtg ggttttagct tgccgctcgc cagggctctc aggggcaacg agaccactgc 360 cgacagcaac gagacaacca cgacctcagg ccctccggac ccgggcgcct cccagccgct 420 gctggcctgg ctgctactgc cgctgctgct cctcctcctc gtgctccttc tcgccgccta 480 cttcttcagg ttcaggaagc agaggaaagc tgtggtcagc accagcgaca agaagatgcc 540 caacggaatc ttggaggagc aagagcagca aagggtgatg ctgctcagca ggtcaccctc 600 agggcccaag aagtattttc ccatccccgt ggagcacctg gaggaggaga tccgtatcag 660 atccgccgac gactgcaagc agtttcggga ggagttcaac tcattgccat ctggacacat 720 acaaggaact tttgaactgg caaataaaga agaaaacaga gaaaaaaaca gatatcccaa 780 catccttccc aatgaccatt ctagggtgat tctgagccaa ctggatggaa ttccctgttc 840 agactacatc aatgcttcct acatagatgg ttacaaagag aagaataaat tcatagcagc 900 tcaaggtccc aaacaggaaa cggttaacga cttctggaga atggtctggg agcaaaagtc 960 tgcgaccatc gtcatgttaa caaacttgaa agaaaggaaa gaggaaaagt gccatcagta 1020 ctggcccgac caaggctgct ggacctatgg aaacatccgg gtgtgcgtgg aggactgcgt 1080 ggttttggtc gactacacca tccggaagtt ctgcatacag ccacagctcc ccgacggctg 1140 caaagccccc aggctggtct cacagctgca cttcaccagc tggcccgact tcggagtgcc 1200 ttttaccccc attgggatgc tgaagttcct caagaaagta aagacgctca accccgtgca 1260 cgctgggccc atcgtggtcc actgtagcgc gggcgtgggc cggacgggca ccttcattgt 1320 gatcgatgcc atgatggcca tgatgcacgc ggagcagaag gtggatgtgt ttgaatttgt 1380 gtctcgaatc cgtaatcagc gccctcagat ggttcaaacg gatatgcagt acacgttcat 1440 ctaccaagcc ttactcgagt actacctcta cggggacaca gagctggacg tgtcctccct 1500 ggagaagcac ctgcagacca tgcacggcac caccacccac ttcgacaaga tcgggctgga 1560 ggaggagttc aggaaattga caaatgtccg gatcatgaag gagaacatga ggacgggcaa 1620 cttgccggca aacatgaaga aggccagggt catccagatc atcccgtatg acttcaaccg 1680 agtgatcctt tccatgaaaa ggggtcaaga atacacagac tacatcaacg catccttcat 1740 agacggctac cgacagaagg actatttcat cgccacccag gggccactgg cacacacggt 1800 tgaggacttc tggaggatga tctgggaatg gaaatcccac actatcgtga tgctgacgga 1860 ggtgcaggag agagagcagg ataaatgcta ccagtattgg ccaaccgagg gctcagttac 1920 tcatggagaa ataacgattg agataaagaa tgataccctt tcagaagcca tcagtatacg 1980 agactttctg gtcactctca atcagcccca ggcccgccag gaggagcagg tccgagtagt 2040 gcgccagttt cacttccacg gctggcctga gatcgggatt cccgccgagg gcaaaggcat 2100 gattgacctc atcgcagccg tgcagaagca gcagcagcag acaggcaacc accccatcac 2160 cgtgcactgc agtgccggag ctgggcgaac aggtacattc atagccctca gcaacatttt 2220 ggagcgagta aaagccgagg gacttttaga tgtatttcaa gctgtgaaga gtttacgact 2280 tcagagacca catatggtgc aaaccctgga acagtatgaa ttctgctaca aagtggtaca 2340 agattttatt gatatatttt ctgattatgc taatttcaaa tgaagattcc tgccttaaaa 2400 tattttttaa tttaatggtc agtatatttt gtaaaaatca tgttaattta tttcatagtt 2460 gacattaata tcttccctaa tttctttgta tatattttgt tatgccttaa aggccacctg 2520 ctatacagtt gttaaatctt aaatatgctt tttaaaaatt ggaataatgt attaaggtca 2580 aataatatcc cataaaatat atatttctgc taatattagt aaatatctta atttttaaaa 2640 aaaaaaaaaa aaaa 2654 <210> SEQ ID NO 793 <211> LENGTH: 700 <212> TYPE: PRT <213> ORGANISM: Homo sapiens <400> SEQUENCE: 793 Met Glu Pro Leu Cys Pro Leu Leu Leu Val Gly Phe Ser Leu Pro Leu 1 5 10 15 Ala Arg Ala Leu Arg Gly Asn Glu Thr Thr Ala Asp Ser Asn Glu Thr 20 25 30 Thr Thr Thr Ser Gly Pro Pro Asp Pro Gly Ala Ser Gln Pro Leu Leu 35 40 45 Ala Trp Leu Leu Leu Pro Leu Leu Leu Leu Leu Leu Val Leu Leu Leu 50 55 60 Ala Ala Tyr Phe Phe Arg Phe Arg Lys Gln Arg Lys Ala Val Val Ser 65 70 75 80 Thr Ser Asp Lys Lys Met Pro Asn Gly Ile Leu Glu Glu Gln Glu Gln 85 90 95 Gln Arg Val Met Leu Leu Ser Arg Ser Pro Ser Gly Pro Lys Lys Tyr 100 105 110 Phe Pro Ile Pro Val Glu His Leu Glu Glu Glu Ile Arg Ile Arg Ser 115 120 125 Ala Asp Asp Cys Lys Gln Phe Arg Glu Glu Phe Asn Ser Leu Pro Ser 130 135 140 Gly His Ile Gln Gly Thr Phe Glu Leu Ala Asn Lys Glu Glu Asn Arg 145 150 155 160 Glu Lys Asn Arg Tyr Pro Asn Ile Leu Pro Asn Asp His Ser Arg Val 165 170 175 Ile Leu Ser Gln Leu Asp Gly Ile Pro Cys Ser Asp Tyr Ile Asn Ala 180 185 190 Ser Tyr Ile Asp Gly Tyr Lys Glu Lys Asn Lys Phe Ile Ala Ala Gln 195 200 205 Gly Pro Lys Gln Glu Thr Val Asn Asp Phe Trp Arg Met Val Trp Glu 210 215 220 Gln Lys Ser Ala Thr Ile Val Met Leu Thr Asn Leu Lys Glu Arg Lys 225 230 235 240 Glu Glu Lys Cys His Gln Tyr Trp Pro Asp Gln Gly Cys Trp Thr Tyr 245 250 255 Gly Asn Ile Arg Val Cys Val Glu Asp Cys Val Val Leu Val Asp Tyr 260 265 270 Thr Ile Arg Lys Phe Cys Ile Gln Pro Gln Leu Pro Asp Gly Cys Lys 275 280 285 Ala Pro Arg Leu Val Ser Gln Leu His Phe Thr Ser Trp Pro Asp Phe 290 295 300 Gly Val Pro Phe Thr Pro Ile Gly Met Leu Lys Phe Leu Lys Lys Val 305 310 315 320 Lys Thr Leu Asn Pro Val His Ala Gly Pro Ile Val Val His Cys Ser 325 330 335 Ala Gly Val Gly Arg Thr Gly Thr Phe Ile Val Ile Asp Ala Met Met 340 345 350 Ala Met Met His Ala Glu Gln Lys Val Asp Val Phe Glu Phe Val Ser 355 360 365 Arg Ile Arg Asn Gln Arg Pro Gln Met Val Gln Thr Asp Met Gln Tyr 370 375 380 Thr Phe Ile Tyr Gln Ala Leu Leu Glu Tyr Tyr Leu Tyr Gly Asp Thr 385 390 395 400 Glu Leu Asp Val Ser Ser Leu Glu Lys His Leu Gln Thr Met His Gly 405 410 415 Thr Thr Thr His Phe Asp Lys Ile Gly Leu Glu Glu Glu Phe Arg Lys 420 425 430 Leu Thr Asn Val Arg Ile Met Lys Glu Asn Met Arg Thr Gly Asn Leu 435 440 445 Pro Ala Asn Met Lys Lys Ala Arg Val Ile Gln Ile Ile Pro Tyr Asp 450 455 460 Phe Asn Arg Val Ile Leu Ser Met Lys Arg Gly Gln Glu Tyr Thr Asp 465 470 475 480 Tyr Ile Asn Ala Ser Phe Ile Asp Gly Tyr Arg Gln Lys Asp Tyr Phe 485 490 495 Ile Ala Thr Gln Gly Pro Leu Ala His Thr Val Glu Asp Phe Trp Arg 500 505 510 Met Ile Trp Glu Trp Lys Ser His Thr Ile Val Met Leu Thr Glu Val 515 520 525 Gln Glu Arg Glu Gln Asp Lys Cys Tyr Gln Tyr Trp Pro Thr Glu Gly 530 535 540 Ser Val Thr His Gly Glu Ile Thr Ile Glu Ile Lys Asn Asp Thr Leu 545 550 555 560 Ser Glu Ala Ile Ser Ile Arg Asp Phe Leu Val Thr Leu Asn Gln Pro 565 570 575 Gln Ala Arg Gln Glu Glu Gln Val Arg Val Val Arg Gln Phe His Phe 580 585 590 His Gly Trp Pro Glu Ile Gly Ile Pro Ala Glu Gly Lys Gly Met Ile 595 600 605 Asp Leu Ile Ala Ala Val Gln Lys Gln Gln Gln Gln Thr Gly Asn His 610 615 620 Pro Ile Thr Val His Cys Ser Ala Gly Ala Gly Arg Thr Gly Thr Phe 625 630 635 640 Ile Ala Leu Ser Asn Ile Leu Glu Arg Val Lys Ala Glu Gly Leu Leu 645 650 655 Asp Val Phe Gln Ala Val Lys Ser Leu Arg Leu Gln Arg Pro His Met 660 665 670 Val Gln Thr Leu Glu Gln Tyr Glu Phe Cys Tyr Lys Val Val Gln Asp 675 680 685 Phe Ile Asp Ile Phe Ser Asp Tyr Ala Asn Phe Lys 690 695 700 <210> SEQ ID NO 794 <211> LENGTH: 2263 <212> TYPE: DNA <213> ORGANISM: Homo sapiens <400> SEQUENCE: 794 ctgagaggct gggtggctgg gcctgggaga cacacagagg ccaggcctta gcgcggctca 60 gccatgagca acaggagtag cttttcccgg ctcacctggt tcaggaagca gaggaaagct 120 gtggtcagca ccagcgacaa gaagatgccc aacggaatct tggaggagca agagcagcaa 180 agggtgatgc tgctcagcag gtcaccctca gggcccaaga agtattttcc catccccgtg 240 gagcacctgg aggaggagat ccgtatcaga tccgccgacg actgcaagca gtttcgggag 300 gagttcaact cattgccatc tggacacata caaggaactt ttgaactggc aaataaagaa 360 gaaaacagag aaaaaaacag atatcccaac atccttccca atgaccattc tagggtgatt 420 ctgagccaac tggatggaat tccctgttca gactacatca atgcttccta catagatggt 480 tacaaagaga agaataaatt catagcagct caaggtccca aacaggaaac ggttaacgac 540 ttctggagaa tggtctggga gcaaaagtct gcgaccatcg tcatgttaac aaacttgaaa 600 gaaaggaaag aggaaaagtg ccatcagtac tggcccgacc aaggctgctg gacctatgga 660 aacatccggg tgtgcgtgga ggactgcgtg gttttggtcg actacaccat ccggaagttc 720 tgcatacagc cacagctccc cgacggctgc aaagccccca ggctggtctc acagctgcac 780 ttcaccagct ggcccgactt cggagtgcct tttaccccca ttgggatgct gaagttcctc 840 aagaaagtaa agacgctcaa ccccgtgcac gctgggccca tcgtggtcca ctgtagcgcg 900 ggcgtgggcc ggacgggcac cttcattgtg atcgatgcca tgatggccat gatgcacgcg 960 gagcagaagg tggatgtgtt tgaatttgtg tctcgaatcc gtaatcagcg ccctcagatg 1020 gttcaaacgg atatgcagta cacgttcatc taccaagcct tactcgagta ctacctctac 1080 ggggacacag agctggacgt gtcctccctg gagaagcacc tgcagaccat gcacggcacc 1140 accacccact tcgacaagat cgggctggag gaggagttca ggaaattgac aaatgtccgg 1200 atcatgaagg agaacatgag gacgggcaac ttgccggcaa acatgaagaa ggccagggtc 1260 atccagatca tcccgtatga cttcaaccga gtgatccttt ccatgaaaag gggtcaagaa 1320 tacacagact acatcaacgc atccttcata gacggctacc gacagaagga ctatttcatc 1380 gccacccagg ggccactggc acacacggtt gaggacttct ggaggatgat ctgggaatgg 1440 aaatcccaca ctatcgtgat gctgacggag gtgcaggaga gagagcagga taaatgctac 1500 cagtattggc caaccgaggg ctcagttact catggagaaa taacgattga gataaagaat 1560 gatacccttt cagaagccat cagtatacga gactttctgg tcactctcaa tcagccccag 1620 gcccgccagg aggagcaggt ccgagtagtg cgccagtttc acttccacgg ctggcctgag 1680 atcgggattc ccgccgaggg caaaggcatg attgacctca tcgcagccgt gcagaagcag 1740 cagcagcaga caggcaacca ccccatcacc gtgcactgca gtgccggagc tgggcgaaca 1800 ggtacattca tagccctcag caacattttg gagcgagtaa aagccgaggg acttttagat 1860 gtatttcaag ctgtgaagag tttacgactt cagagaccac atatggtgca aaccctggaa 1920 cagtatgaat tctgctacaa agtggtacaa gattttattg atatattttc tgattatgct 1980 aatttcaaat gaagattcct gccttaaaat attttttaat ttaatggtca gtatattttg 2040 taaaaatcat gttaatttat ttcatagttg acattaatat cttccctaat ttctttgtat 2100 atattttgtt atgccttaaa ggccacctgc tatacagttg ttaaatctta aatatgcttt 2160 ttaaaaattg gaataatgta ttaaggtcaa ataatatccc ataaaatata tatttctgct 2220 aatattagta aatatcttaa tttttaaaaa aaaaaaaaaa aaa 2263 <210> SEQ ID NO 795 <211> LENGTH: 642 <212> TYPE: PRT <213> ORGANISM: Homo sapiens <400> SEQUENCE: 795 Met Ser Asn Arg Ser Ser Phe Ser Arg Leu Thr Trp Phe Arg Lys Gln 1 5 10 15 Arg Lys Ala Val Val Ser Thr Ser Asp Lys Lys Met Pro Asn Gly Ile 20 25 30 Leu Glu Glu Gln Glu Gln Gln Arg Val Met Leu Leu Ser Arg Ser Pro 35 40 45 Ser Gly Pro Lys Lys Tyr Phe Pro Ile Pro Val Glu His Leu Glu Glu 50 55 60 Glu Ile Arg Ile Arg Ser Ala Asp Asp Cys Lys Gln Phe Arg Glu Glu 65 70 75 80 Phe Asn Ser Leu Pro Ser Gly His Ile Gln Gly Thr Phe Glu Leu Ala 85 90 95 Asn Lys Glu Glu Asn Arg Glu Lys Asn Arg Tyr Pro Asn Ile Leu Pro 100 105 110 Asn Asp His Ser Arg Val Ile Leu Ser Gln Leu Asp Gly Ile Pro Cys 115 120 125 Ser Asp Tyr Ile Asn Ala Ser Tyr Ile Asp Gly Tyr Lys Glu Lys Asn 130 135 140 Lys Phe Ile Ala Ala Gln Gly Pro Lys Gln Glu Thr Val Asn Asp Phe 145 150 155 160 Trp Arg Met Val Trp Glu Gln Lys Ser Ala Thr Ile Val Met Leu Thr 165 170 175 Asn Leu Lys Glu Arg Lys Glu Glu Lys Cys His Gln Tyr Trp Pro Asp 180 185 190 Gln Gly Cys Trp Thr Tyr Gly Asn Ile Arg Val Cys Val Glu Asp Cys 195 200 205 Val Val Leu Val Asp Tyr Thr Ile Arg Lys Phe Cys Ile Gln Pro Gln 210 215 220 Leu Pro Asp Gly Cys Lys Ala Pro Arg Leu Val Ser Gln Leu His Phe 225 230 235 240 Thr Ser Trp Pro Asp Phe Gly Val Pro Phe Thr Pro Ile Gly Met Leu 245 250 255 Lys Phe Leu Lys Lys Val Lys Thr Leu Asn Pro Val His Ala Gly Pro 260 265 270 Ile Val Val His Cys Ser Ala Gly Val Gly Arg Thr Gly Thr Phe Ile 275 280 285 Val Ile Asp Ala Met Met Ala Met Met His Ala Glu Gln Lys Val Asp 290 295 300 Val Phe Glu Phe Val Ser Arg Ile Arg Asn Gln Arg Pro Gln Met Val 305 310 315 320 Gln Thr Asp Met Gln Tyr Thr Phe Ile Tyr Gln Ala Leu Leu Glu Tyr 325 330 335 Tyr Leu Tyr Gly Asp Thr Glu Leu Asp Val Ser Ser Leu Glu Lys His 340 345 350 Leu Gln Thr Met His Gly Thr Thr Thr His Phe Asp Lys Ile Gly Leu 355 360 365 Glu Glu Glu Phe Arg Lys Leu Thr Asn Val Arg Ile Met Lys Glu Asn 370 375 380 Met Arg Thr Gly Asn Leu Pro Ala Asn Met Lys Lys Ala Arg Val Ile 385 390 395 400 Gln Ile Ile Pro Tyr Asp Phe Asn Arg Val Ile Leu Ser Met Lys Arg 405 410 415 Gly Gln Glu Tyr Thr Asp Tyr Ile Asn Ala Ser Phe Ile Asp Gly Tyr 420 425 430 Arg Gln Lys Asp Tyr Phe Ile Ala Thr Gln Gly Pro Leu Ala His Thr 435 440 445 Val Glu Asp Phe Trp Arg Met Ile Trp Glu Trp Lys Ser His Thr Ile 450 455 460 Val Met Leu Thr Glu Val Gln Glu Arg Glu Gln Asp Lys Cys Tyr Gln 465 470 475 480 Tyr Trp Pro Thr Glu Gly Ser Val Thr His Gly Glu Ile Thr Ile Glu 485 490 495 Ile Lys Asn Asp Thr Leu Ser Glu Ala Ile Ser Ile Arg Asp Phe Leu 500 505 510 Val Thr Leu Asn Gln Pro Gln Ala Arg Gln Glu Glu Gln Val Arg Val 515 520 525 Val Arg Gln Phe His Phe His Gly Trp Pro Glu Ile Gly Ile Pro Ala 530 535 540 Glu Gly Lys Gly Met Ile Asp Leu Ile Ala Ala Val Gln Lys Gln Gln 545 550 555 560 Gln Gln Thr Gly Asn His Pro Ile Thr Val His Cys Ser Ala Gly Ala 565 570 575 Gly Arg Thr Gly Thr Phe Ile Ala Leu Ser Asn Ile Leu Glu Arg Val 580 585 590 Lys Ala Glu Gly Leu Leu Asp Val Phe Gln Ala Val Lys Ser Leu Arg 595 600 605 Leu Gln Arg Pro His Met Val Gln Thr Leu Glu Gln Tyr Glu Phe Cys 610 615 620 Tyr Lys Val Val Gln Asp Phe Ile Asp Ile Phe Ser Asp Tyr Ala Asn 625 630 635 640 Phe Lys <210> SEQ ID NO 796 <211> LENGTH: 844 <212> TYPE: DNA <213> ORGANISM: Homo sapiens <400> SEQUENCE: 796 gcacgagctg cagagggagg cggcactggt ctcgacgtgg ggcggccagc gatgaagccg 60 cccagttcaa tacaaacaag tgagtttgac tcatcagatg aagagcctat tgaagatgaa 120 cagactccaa ttcatatatc atggctatct ttgtcacgag tgaattgttc tcagtttctc 180 ggtttatgtg ctcttccagg ttgtaaattt aaagatgtta gaagaaatgt ccaaaaagat 240 acagaagaac taaagagctg tggtatacaa gacatatttg ttttctgcac cagaggggaa 300 ctgtcaaaat atagagtccc aaaccttctg gatctctacc agcaatgtgg aattatcacc 360 catcatcatc caatcgcaga tggagggact cctgacatag ccagctgctg tgaaataatg 420 gaagagctta caacctgcct taaaaattac cgaaaaacct taatacactg ctatggagga 480 cttgggagat cttgtcttgt agctgcttgt ctcctactat acctgtctga cacaatatca 540 ccagagcaag ccatagacag cctgcgagac ctaagaggat ccggggcaat acagaccatc 600 aagcaataca attatcttca tgagtttcgg gacaaattag ctgcacatct atcatcaaga 660 gattcacaat caagatctgt atcaagataa aggaattcaa atagcatata tatgaccatg 720 tctgaaatgt cagttctcta gcataatttg tattgaaatg aaaccaccag tgttatcaac 780 ttgaatgtaa atgtacatgt gcagatattc ctaaagtttt attgacaaaa aaaaaaaaaa 840 aaaa 844 <210> SEQ ID NO 797 <211> LENGTH: 212 <212> TYPE: PRT <213> ORGANISM: Homo sapiens <400> SEQUENCE: 797 Met Lys Pro Pro Ser Ser Ile Gln Thr Ser Glu Phe Asp Ser Ser Asp 1 5 10 15 Glu Glu Pro Ile Glu Asp Glu Gln Thr Pro Ile His Ile Ser Trp Leu 20 25 30 Ser Leu Ser Arg Val Asn Cys Ser Gln Phe Leu Gly Leu Cys Ala Leu 35 40 45 Pro Gly Cys Lys Phe Lys Asp Val Arg Arg Asn Val Gln Lys Asp Thr 50 55 60 Glu Glu Leu Lys Ser Cys Gly Ile Gln Asp Ile Phe Val Phe Cys Thr 65 70 75 80 Arg Gly Glu Leu Ser Lys Tyr Arg Val Pro Asn Leu Leu Asp Leu Tyr 85 90 95 Gln Gln Cys Gly Ile Ile Thr His His His Pro Ile Ala Asp Gly Gly 100 105 110 Thr Pro Asp Ile Ala Ser Cys Cys Glu Ile Met Glu Glu Leu Thr Thr 115 120 125 Cys Leu Lys Asn Tyr Arg Lys Thr Leu Ile His Cys Tyr Gly Gly Leu 130 135 140 Gly Arg Ser Cys Leu Val Ala Ala Cys Leu Leu Leu Tyr Leu Ser Asp 145 150 155 160 Thr Ile Ser Pro Glu Gln Ala Ile Asp Ser Leu Arg Asp Leu Arg Gly 165 170 175 Ser Gly Ala Ile Gln Thr Ile Lys Gln Tyr Asn Tyr Leu His Glu Phe 180 185 190 Arg Asp Lys Leu Ala Ala His Leu Ser Ser Arg Asp Ser Gln Ser Arg 195 200 205 Ser Val Ser Arg 210 <210> SEQ ID NO 798 <211> LENGTH: 1396 <212> TYPE: DNA <213> ORGANISM: Homo sapiens <400> SEQUENCE: 798 tgactatcca gctctgagag acgggagttt ggagttgccc gctttacttt ggttgggttg 60 gggggggcgg cgggctgttt tgttcctttt cttttttaag agttgggttt tcttttttaa 120 ttatccaaac agtgggcagc ttcctccccc acacccaagt atttgcacaa tatttgtgcg 180 gggtatgggg gtgggttttt aaatctcgtt tctcttggac aagcacaggg atctcgttct 240 cctcattttt tgggggtgtg tggggacttc tcaggtcgtg tccccagcct tctctgcagt 300 cccttctgcc ctgccgggcc cgtcgggagg cgccatggct cggatgaacc gcccggcccc 360 ggtggaggtg agctacaaac acatgcgctt cctcatcacc cacaacccca ccaacgccac 420 gctcagcacc ttcattgagg acctgaagaa gtacggggct accactgtgg tgcgtgtgtg 480 tgaagtgacc tatgacaaaa cgccgctgga gaaggatggc atcaccgttg tggactggcc 540 gtttgacgat ggggcgcccc cgcccggcaa ggtagtggaa gactggctga gcctggtgaa 600 ggccaagttc tgtgaggccc ccggcagctg cgtggctgtg cactgcgtgg cgggcctggg 660 ccgggctcca gtccttgtgg cgctggcgct tattgagagc gggatgaagt acgaggacgc 720 catccagttc atccgccaga agcgccgcgg agccatcaac agcaagcagc tcacctacct 780 ggagaaatac cggcccaaac agaggctgcg gttcaaagac ccacacacgc acaagacccg 840 gtgctgcgtt atgtagctca ggaccttggc tgggcctggt cgtcatgtag gtcaggacct 900 tggctggacc tggaggccct gcccagccct gctctgccca gcccagcagg ggctccaggc 960 cttggctggc cccacatcgc cttttcctcc ccgacacctc cgtgcacttg tgtccgagga 1020 gcgaggagcc cctcgggccc tgggtggcct ctgggccctt tctcctgtct ccgccactcc 1080 ctctggcggc gctggccgtg gctctgtctc tctgaggtgg gtcgggcgcc ctctgcccgc 1140 cccctcccac accagccagg ctggtctcct ctagcctgtt tgttgtgggg tgggggtata 1200 ttttgtaacc actgggcccc cagcccctct tttgcgaccc cttgtcctga cctgttctcg 1260 gcaccttaaa ttattagacc ccggggcagt caggtgctcc ggacacccga aggcaataaa 1320 acaggagccg tgaaaaaaaa aaaaaaaaaa aaaaaaaaaa aaaaaaaaaa aaaaaaaaaa 1380 aaaaaaaaaa aaaaaa 1396 <210> SEQ ID NO 799 <211> LENGTH: 173 <212> TYPE: PRT <213> ORGANISM: Homo sapiens <400> SEQUENCE: 799 Met Ala Arg Met Asn Arg Pro Ala Pro Val Glu Val Ser Tyr Lys His 1 5 10 15 Met Arg Phe Leu Ile Thr His Asn Pro Thr Asn Ala Thr Leu Ser Thr 20 25 30 Phe Ile Glu Asp Leu Lys Lys Tyr Gly Ala Thr Thr Val Val Arg Val 35 40 45 Cys Glu Val Thr Tyr Asp Lys Thr Pro Leu Glu Lys Asp Gly Ile Thr 50 55 60 Val Val Asp Trp Pro Phe Asp Asp Gly Ala Pro Pro Pro Gly Lys Val 65 70 75 80 Val Glu Asp Trp Leu Ser Leu Val Lys Ala Lys Phe Cys Glu Ala Pro 85 90 95 Gly Ser Cys Val Ala Val His Cys Val Ala Gly Leu Gly Arg Ala Pro 100 105 110 Val Leu Val Ala Leu Ala Leu Ile Glu Ser Gly Met Lys Tyr Glu Asp 115 120 125 Ala Ile Gln Phe Ile Arg Gln Lys Arg Arg Gly Ala Ile Asn Ser Lys 130 135 140 Gln Leu Thr Tyr Leu Glu Lys Tyr Arg Pro Lys Gln Arg Leu Arg Phe 145 150 155 160 Lys Asp Pro His Thr His Lys Thr Arg Cys Cys Val Met 165 170 <210> SEQ ID NO 800 <211> LENGTH: 3925 <212> TYPE: DNA <213> ORGANISM: Homo sapiens <400> SEQUENCE: 800 agcggggctg cgcgaagtca tcgctgttcc agacagcgat gactcgagag cggtgggggt 60 ggcggcgcga tcggccgggc tgtaaccgtc gtctgtccgg gagcggctgg agcggcagcg 120 gcggccgggc acggcgcgag gtgacgccac agggcagcgg cggcagcgga ggcagcggcg 180 gcagcaggag acgcagcggc ggccgcagca gcagcagcaa gacggactcg tggagacgcg 240 ccgccgccgc cgccgccggg ccgggccggg tgtcgcgcgc cgaggctggg ggggagtcgt 300 cgccgccgcc gccaccgcta ccgccgccgc cgccgccgcc gaggtgactg aggagagagg 360 cgcctcctcg ctcccgccac cgccggactt caatgcccag tccccagctc gccagcgttt 420 ttcgttggaa tatacgttgc acatttatgg cgattctgag tgtgagggca gacttctgcc 480 aggctcagca cagcattttc gctgacaagt gagcttggag gttctatgtg ccataattaa 540 cattgccttg aagactcctg gacaccgaga ctggcctcag aaatagttgg cttttttttt 600 tttttaattg caagcatatt tcttttaatg actccagtaa aattaagcat caagtaaaca 660 agtggaaagt gacctacact tttaacttgt ctcactagtg cctaaatgta gtaaaggctg 720 cttaagtttt gtatgtagtt ggattttttg gagtccgaat atttccatct gcagaaattg 780 aggcccaaat tgaatttgga ttcaagtgga ttctaaatac tttgcttatc ttgaagagag 840 aagcttcata aggaataaac aagttgaata gagaaaacac tgattgataa taggcatttt 900 agtggtcttt ttaatgtttt ctgctgtgaa acatttcaag atttattgat tttttttttt 960 cactttcccc atcacactca cacgcacgct cacacttttt atttgccata atgaaccgtc 1020 cagcccctgt ggagatctcc tatgagaaca tgcgttttct gataactcac aaccctacca 1080 atgctactct caacaagttc acagaggaac ttaagaagta tggagtgacg actttggttc 1140 gagtttgtga tgctacatat gataaagctc cagttgaaaa agaaggaatc cacgttctag 1200 attggccatt tgatgatgga gctccacccc ctaatcagat agtagatgat tggttaaacc 1260 tgttaaaaac caaatttcgt gaagagccag gttgctgtgt tgcagtgcat tgtgttgcag 1320 gattgggaag ggcacctgtg ctggttgcac ttgctttgat tgaatgtgga atgaagtacg 1380 aagatgcagt tcagtttata agacaaaaaa gaaggggagc gttcaattcc aaacagctgc 1440 tttatttgga gaaataccga cctaagatgc gattacgctt cagagatacc aatgggcatt 1500 gctgtgttca gtagaaggaa atgtaaacga aggctgactt gattgtgcca tttagaggga 1560 actcttggta cctggaaatg tgaatctgga atattacctg tgtcatcaaa gtagtgatgg 1620 attcagtact cctcaaccac tctcctaatg attggaacaa aagcaaacaa aaaagaaatc 1680 tctctataaa atgaataaaa tgtttaagaa aagagaaaga gaaaaggaat taattcagtg 1740 aaggatgatt ttgctcctag ttttggagtt tgaatttctg ccaggattga attattttga 1800 aatctcctgt ctttttaaac tttttcaaaa taggtctcta aggaaaacca gcagaacatt 1860 aggcctgtgc aaaaccatct gtttggggag cacactcttc cattatgctt ggcacataga 1920 tctccctgtg gtgggatttt ttttttccct ttttttgtgg gggagggttg gtggtatatt 1980 tttcccctct tttttccttc ctctcctaca tctccctttt cccccgatcc aagttgtaga 2040 tggaatagaa gcccttgttg ctgtagatgt gcgtgcagtc tggcagcctt aagcccacct 2100 gggcactttt agataaaaaa aaaaaaaaac aaaaaacaac accaaaaaaa cagcagtgat 2160 atatatattc caggtggttt ttagtcttta ctgatgaaag ggtgttcatg ttagtttctt 2220 caaaacccta tctaatacta ggcaaagtag ccaagagcct tttgttttgt ttttattttg 2280 ataaattagt ggagaaatgg cattttaaga ggagtctctt ctcaacttac ctgagagtcg 2340 aattcttctc ttccctaacc aatgaagcta agtggttatc ccagaaactt gtcttctaaa 2400 agggaggact ccaggccatc aataaagatg tccaggcagt gagcgtactt tttacaccct 2460 gtagaattgt gggctgtagc gttactctga ttttctgtct agtatcagag aatgctggta 2520 gcttaaaatt tttattttag gacttgtact ctgaattttc aggaaccgtc aaaggagcag 2580 cagcaaattc acatattttc gacttgagaa atgcttgtgg tatgtgtttt ccaaactgcc 2640 ccctatatgt aaagttcagt ttaaccactg attgccttgt tattactagg ttttttgaga 2700 ttaaaaaaaa aaaatccctg gtttaaaacc aacaatgatg cctagtgagt atgtgtccac 2760 aggccataac agggtagaag agagacatcg tgcaacccaa tgagtagtga agggactgtg 2820 ttgcttgtga agcggtgtag tagcattttt gcagattctt ggctgggttt agtgtactga 2880 tctagaaaag ctgtttttct gctcctttgt ggaaggcagt tatgatcagg ctgcatggac 2940 aaagcaggta gaggggcacc atcaggggct cttgcactat tttcacctct aaatattacg 3000 tactcagtag tgccctgctt ctagggctct gaatacgggc ttaaagtcat cttgtcctgc 3060 tggaatttgc tgtgcagagc cataagcctc ccattttgtt agcgtcagct aggccaatag 3120 gaacagaccg ggaccttgtc tcacactgat gatacctcac atgttgaccg gctatgtgaa 3180 ctgcctattt cctatgctgg agttttgatt tttaactaaa cgcaaatctg tagattctct 3240 cctctcccat cccagaaaac aaaacaaaat aatgcttttc gaaattgttt ctaggacttt 3300 aaaacataat ggtatatcca aaattcttta tttcagaatg caacaataga ttccattaat 3360 atagactcaa gatcaaaaca gcatacctgc taagctaaga tagatggtgt tgattccact 3420 gggttttgat caatacaata acaaaccttt ttcctttgac atactctgaa ttttgttgtt 3480 tggggggagg gggtgtgtgt gtgtgtgtgt gtgtgtgtgt gtattgtgtg tgtgtgtgtg 3540 tgcacgcgca gtgtccatca gtatcagtgc ctgcctgagt taggaaaatt acattcctgg 3600 ttctgtattg aggagaagga tgtataaagc aacatgaaac attagccctc cttttatttt 3660 aaagactaat gttaattgtt cttaaaactg gatttttttt ccttaaagca atttttttct 3720 tttcgattta atgaagtatt gctagctgaa gccagtttga catagagaga tgtcagattg 3780 atttgaaagg tgtgcagcct gatttaaaac caaaccctga acccttttaa agaacaataa 3840 aacatatttt acacgctcaa aaaaaaaaaa aaaaaaaaaa aaaaaaaaaa aaaaaaaaaa 3900 aaaaaaaaaa aaaaaaaaaa aaaaa 3925 <210> SEQ ID NO 801 <211> LENGTH: 167 <212> TYPE: PRT <213> ORGANISM: Homo sapiens <400> SEQUENCE: 801 Met Asn Arg Pro Ala Pro Val Glu Ile Ser Tyr Glu Asn Met Arg Phe 1 5 10 15 Leu Ile Thr His Asn Pro Thr Asn Ala Thr Leu Asn Lys Phe Thr Glu 20 25 30 Glu Leu Lys Lys Tyr Gly Val Thr Thr Leu Val Arg Val Cys Asp Ala 35 40 45 Thr Tyr Asp Lys Ala Pro Val Glu Lys Glu Gly Ile His Val Leu Asp 50 55 60 Trp Pro Phe Asp Asp Gly Ala Pro Pro Pro Asn Gln Ile Val Asp Asp 65 70 75 80 Trp Leu Asn Leu Leu Lys Thr Lys Phe Arg Glu Glu Pro Gly Cys Cys 85 90 95 Val Ala Val His Cys Val Ala Gly Leu Gly Arg Ala Pro Val Leu Val 100 105 110 Ala Leu Ala Leu Ile Glu Cys Gly Met Lys Tyr Glu Asp Ala Val Gln 115 120 125 Phe Ile Arg Gln Lys Arg Arg Gly Ala Phe Asn Ser Lys Gln Leu Leu 130 135 140 Tyr Leu Glu Lys Tyr Arg Pro Lys Met Arg Leu Arg Phe Arg Asp Thr 145 150 155 160 Asn Gly His Cys Cys Val Gln 165 <210> SEQ ID NO 802 <211> LENGTH: 1785 <212> TYPE: DNA <213> ORGANISM: Homo sapiens <400> SEQUENCE: 802 atggcagcgg agtcagggga actaatcggg gcttgtgagt tcatgaaaga tcggttatat 60 tttgctactt taaggaatag accaaaaagc acagtaaata cccactattt ctccatcgat 120 gaggagctgg tctatgaaaa tttctatgca gattttggac cgctgaactt ggcaatggtg 180 tacagatatt gctgcaaact aaacaagaaa ctaaaatcat acagtttgtc aagaaagaaa 240 atagtgcact acacctgttt tgaccaacgg aaaagagcaa atgcagcatt tttgataggt 300 gcctatgcag taatctattt aaagaagaca ccagaagaag cctacagagc actcctgtct 360 ggctcaaacc ccccctatct tccattcagg gatgcttcct ttggaaattg cacttacaat 420 ctcaccattc tcgactgttt gcagggaatc agaaagggat tacaacatgg attttttgac 480 tttgagacat ttgatgtgga tgaatatgaa cattatgagc gagttgaaaa tggtgacttc 540 aactggattg ttccaggaaa atttttagca tttagtggac cacatcctaa aagcaaaatt 600 gagaatggtt atcctcttca cgcccctgaa gcctactttc cttatttcaa aaagcataat 660 gtgactgcag ttgtgaggct aaacaaaaag atttatgagg caaagcgctt cacagacgct 720 ggcttcgagc actatgacct cttcttcata gatggcagca cacccagtga caacatcgtg 780 cgaaggttcc tgaacatctg tgagaacacc gaaggggcca tcgccgttca ctgcaaagct 840 ggtcttggaa gaacagggac attgatagcc tgttatgtaa tgaaacacta caggtttaca 900 catgctgaaa taattgcttg gattagaata tgccggccag gctctattat aggaccccag 960 cagcacttcc tggaagaaaa acaagcatcg ttgtgggtcc aaggagacat tttccgatcc 1020 aaactgaaaa atcgaccatc cagtgaagga agtattaata aaattctttc tggcctagat 1080 gatatgtcta ttggtggaaa tctttcaaaa acacaaaaca tggaacgatt tggagaggat 1140 aacttagaag atgatgatgt ggaaatgaaa aatggtataa cccagggaga caaactacgt 1200 gccttaaaaa gtcagagaca gccacgtacc tcaccatcct gtgcatttag gtcagatgat 1260 acaaaaggac atccaagagc agtgtcccag cctttcagat taagttcatc cctgcaagga 1320 tctgcagtta ctttgaagac atcaaaaatg gcactgtccc cttcagcaac ggccaagagg 1380 atcaacagaa cttctttgtc ttcgggtgcc actgtaagaa gcttttccat aaactcccgg 1440 ctagccagtt ctctagggaa cttgaatgct gcaacagatg atccagagaa caaaaagacc 1500 tcctcatcct ctaaggcagg cttcacagcc agcccgttta ccaacctctt gaatggcagc 1560 tcccagccaa ctaccagaaa ttaccctgag ctcaacaata atcagtacaa cagaagcagc 1620 aacagcaacg ggggcaacct gaacagcccc ccaggccccc acagcgccaa gacagaggag 1680 cacaccacca tcctccgacc ctcctacacc gggctttctt cttcttcagc gagattcctg 1740 agccgttcta tcccttccct tcagtctgaa tatgttcatt actaa 1785 <210> SEQ ID NO 803 <211> LENGTH: 594 <212> TYPE: PRT <213> ORGANISM: Homo sapiens <400> SEQUENCE: 803 Met Ala Ala Glu Ser Gly Glu Leu Ile Gly Ala Cys Glu Phe Met Lys 1 5 10 15 Asp Arg Leu Tyr Phe Ala Thr Leu Arg Asn Arg Pro Lys Ser Thr Val 20 25 30 Asn Thr His Tyr Phe Ser Ile Asp Glu Glu Leu Val Tyr Glu Asn Phe 35 40 45 Tyr Ala Asp Phe Gly Pro Leu Asn Leu Ala Met Val Tyr Arg Tyr Cys 50 55 60 Cys Lys Leu Asn Lys Lys Leu Lys Ser Tyr Ser Leu Ser Arg Lys Lys 65 70 75 80 Ile Val His Tyr Thr Cys Phe Asp Gln Arg Lys Arg Ala Asn Ala Ala 85 90 95 Phe Leu Ile Gly Ala Tyr Ala Val Ile Tyr Leu Lys Lys Thr Pro Glu 100 105 110 Glu Ala Tyr Arg Ala Leu Leu Ser Gly Ser Asn Pro Pro Tyr Leu Pro 115 120 125 Phe Arg Asp Ala Ser Phe Gly Asn Cys Thr Tyr Asn Leu Thr Ile Leu 130 135 140 Asp Cys Leu Gln Gly Ile Arg Lys Gly Leu Gln His Gly Phe Phe Asp 145 150 155 160 Phe Glu Thr Phe Asp Val Asp Glu Tyr Glu His Tyr Glu Arg Val Glu 165 170 175 Asn Gly Asp Phe Asn Trp Ile Val Pro Gly Lys Phe Leu Ala Phe Ser 180 185 190 Gly Pro His Pro Lys Ser Lys Ile Glu Asn Gly Tyr Pro Leu His Ala 195 200 205 Pro Glu Ala Tyr Phe Pro Tyr Phe Lys Lys His Asn Val Thr Ala Val 210 215 220 Val Arg Leu Asn Lys Lys Ile Tyr Glu Ala Lys Arg Phe Thr Asp Ala 225 230 235 240 Gly Phe Glu His Tyr Asp Leu Phe Phe Ile Asp Gly Ser Thr Pro Ser 245 250 255 Asp Asn Ile Val Arg Arg Phe Leu Asn Ile Cys Glu Asn Thr Glu Gly 260 265 270 Ala Ile Ala Val His Cys Lys Ala Gly Leu Gly Arg Thr Gly Thr Leu 275 280 285 Ile Ala Cys Tyr Val Met Lys His Tyr Arg Phe Thr His Ala Glu Ile 290 295 300 Ile Ala Trp Ile Arg Ile Cys Arg Pro Gly Ser Ile Ile Gly Pro Gln 305 310 315 320 Gln His Phe Leu Glu Glu Lys Gln Ala Ser Leu Trp Val Gln Gly Asp 325 330 335 Ile Phe Arg Ser Lys Leu Lys Asn Arg Pro Ser Ser Glu Gly Ser Ile 340 345 350 Asn Lys Ile Leu Ser Gly Leu Asp Asp Met Ser Ile Gly Gly Asn Leu 355 360 365 Ser Lys Thr Gln Asn Met Glu Arg Phe Gly Glu Asp Asn Leu Glu Asp 370 375 380 Asp Asp Val Glu Met Lys Asn Gly Ile Thr Gln Gly Asp Lys Leu Arg 385 390 395 400 Ala Leu Lys Ser Gln Arg Gln Pro Arg Thr Ser Pro Ser Cys Ala Phe 405 410 415 Arg Ser Asp Asp Thr Lys Gly His Pro Arg Ala Val Ser Gln Pro Phe 420 425 430 Arg Leu Ser Ser Ser Leu Gln Gly Ser Ala Val Thr Leu Lys Thr Ser 435 440 445 Lys Met Ala Leu Ser Pro Ser Ala Thr Ala Lys Arg Ile Asn Arg Thr 450 455 460 Ser Leu Ser Ser Gly Ala Thr Val Arg Ser Phe Ser Ile Asn Ser Arg 465 470 475 480 Leu Ala Ser Ser Leu Gly Asn Leu Asn Ala Ala Thr Asp Asp Pro Glu 485 490 495 Asn Lys Lys Thr Ser Ser Ser Ser Lys Ala Gly Phe Thr Ala Ser Pro 500 505 510 Phe Thr Asn Leu Leu Asn Gly Ser Ser Gln Pro Thr Thr Arg Asn Tyr 515 520 525 Pro Glu Leu Asn Asn Asn Gln Tyr Asn Arg Ser Ser Asn Ser Asn Gly 530 535 540 Gly Asn Leu Asn Ser Pro Pro Gly Pro His Ser Ala Lys Thr Glu Glu 545 550 555 560 His Thr Thr Ile Leu Arg Pro Ser Tyr Thr Gly Leu Ser Ser Ser Ser 565 570 575 Ala Arg Phe Leu Ser Arg Ser Ile Pro Ser Leu Gln Ser Glu Tyr Val 580 585 590 His Tyr <210> SEQ ID NO 804 <211> LENGTH: 2646 <212> TYPE: DNA <213> ORGANISM: Homo sapiens <220> FEATURE: <221> NAME/KEY: misc_feature <222> LOCATION: 2300 <223> OTHER INFORMATION: n = A,T,C or G <400> SEQUENCE: 804 atgaagcgga aaagcgagcg gcggtcgagc tgggccgccg cgcccccctg ctcgcggcgc 60 tgctcgtcga cctcgccggg tgtgaagaag atccgcagct ccacgcagca agacccgcgc 120 cgccgggacc cccaggacga cgtgtacctg gacatcaccg atcgcctttg ttttgccatt 180 ctctacagca gaccaaagag tgcatcaaat gtacattatt tcagcataga taatgaactt 240 gaatatgaga acttctacgc agattttgga ccactcaatc tggcaatggt ttacagatat 300 tgttgcaaga tcaataagaa attaaagtcc attacaatgt taaggaagaa aattgttcat 360 tttactggct ctgatcagag aaaacaagca aatgctgcct tccttgttgg atgctacatg 420 gttatatatt tggggagaac cccagaagaa gcatatagaa tattaatctt tggagagaca 480 tcctatattc ctttcagaga tgctgcctat ggaagttgca atttctacat tacacttctt 540 gactgttttc atgcagtaaa gaaggcaatg cagtatggct tccttaattt caactcattt 600 aaccttgatg aatatgaaca ctatgaaaaa gcagaaaatg gagatttaaa ttggataata 660 ccagaccgat ttattgcctt ctgtggacct cattcaagag ccagacttga aagtggttac 720 caccaacatt ctcctgagac ttatattcaa tattttaaga atcacaatgt tactaccatt 780 attcgtctga ataaaaggat gtatgatgcc aaacgcttta cggatgctgg cttcgatcac 840 catgatcttt tctttgcgga tggcagcacc cctactgatg ccattgtcaa agaattccta 900 gatatctgtg aaaatgctga gggtgccatt gcagtacatt gcaaagctgg ccttggtcgc 960 acgggcactc tgatagcctg ctacatcatg aagcattaca ggatgacagc agccgagacc 1020 attgcgtggg tcaggatctg cagacctggc tcggtgattg ggcctcagca gcagtttttg 1080 gtgatgaagc aaaccaacct ctggctggaa ggggactatt ttcgtcagaa gttaaagggg 1140 caggagaatg gacaacacag agcagccttc tccaaacttc tctctggcgt tgatgacatt 1200 tccataaatg gggtcgagaa tcaagatcag caagaacccg aaccgtacag tgatgatgac 1260 gaaatcaatg gagtgacaca aggtgataga cttcgggcct tgaaaagcag aagacaatcc 1320 aaaacaaacg ctattcctct cactctctcc atttcaagga ctaaaacagt cttgcgttaa 1380 gtaaaaacct gtgaccagag ctgaaggaag actctaggac tgaaaactgc aacagaaatt 1440 agcacaattt gaaaacaaaa caaaattgca aaagccttag ttgctttttc cacctaagaa 1500 gttgatcaat ggagaaaatg tccactggag tttgaataat gaactttgag tttgggtgca 1560 agcaaatgac tcagagaagg gtccagctct caagctgaat gacaaacatg ctgttgtaaa 1620 tttagtctca ggtgtaaata cccaagccct ctggtaccca gggagctggc tggtctgtgg 1680 tgcatgtgtg tccctgtgat ggcaatcatt gtagttgctg gccttcagaa gaattgagga 1740 tctgatggag gttttttatg tatttatttt ctgttcacct tgtgaccctg tgtcaaaatt 1800 tataaagata caaaaggcat tactgaaatg gtactttctg taatttgata ctatttggct 1860 taatcatctt cacttgacta tttgtaatac tgttgtaatg ttaactctgt taagtaccca 1920 agctgcttgt cttccaccaa agagtgcttt attaacaaga atctgtgaaa atcacattta 1980 aacactgttg catgttgtaa gaccaggtgg taccttagta acctaaaact tgcaagagaa 2040 tattaatggt agctttagaa gactcaggag gagaaactga cttcagagtt ggaagatgtt 2100 gcaagtcgtt cctttttctg tccttcaggg actgaagaac tgggaggctg cccattgttt 2160 ggttgccagt catacaaatt aaaatcatat ttccttccat gaatggaaga aacacactat 2220 tggtttttcc ccttggaaac agcaatccca aataatgtcg gcttacaaaa aaaaaagtta 2280 ccactttttt agagtccttn ccctgtaaca ttggattttt ttttccctta tgagatccac 2340 ctaaggccat tgacgtggcc tgcgatctca gtgacaatga tctgctttct ggatctcact 2400 gttgcctttg gttagggaac acagagtgct tctcccgcag ccctactgga acacagcaga 2460 gtctgtgcca tgaagcagtt acagaaacag aattgatgtg ctgctaaaaa aaaaaaaaaa 2520 aatggggccc gggggggcgt ccgccggccc tgcgggccgc cggtgaaata ccactactct 2580 gatcgttttt tcactgaccc ggtgaggcgg gggggcgagc cccgaggggc tctcgcttct 2640 ggcgcg 2646 <210> SEQ ID NO 805 <211> LENGTH: 459 <212> TYPE: PRT <213> ORGANISM: Homo sapiens <400> SEQUENCE: 805 Met Lys Arg Lys Ser Glu Arg Arg Ser Ser Trp Ala Ala Ala Pro Pro 1 5 10 15 Cys Ser Arg Arg Cys Ser Ser Thr Ser Pro Gly Val Lys Lys Ile Arg 20 25 30 Ser Ser Thr Gln Gln Asp Pro Arg Arg Arg Asp Pro Gln Asp Asp Val 35 40 45 Tyr Leu Asp Ile Thr Asp Arg Leu Cys Phe Ala Ile Leu Tyr Ser Arg 50 55 60 Pro Lys Ser Ala Ser Asn Val His Tyr Phe Ser Ile Asp Asn Glu Leu 65 70 75 80 Glu Tyr Glu Asn Phe Tyr Ala Asp Phe Gly Pro Leu Asn Leu Ala Met 85 90 95 Val Tyr Arg Tyr Cys Cys Lys Ile Asn Lys Lys Leu Lys Ser Ile Thr 100 105 110 Met Leu Arg Lys Lys Ile Val His Phe Thr Gly Ser Asp Gln Arg Lys 115 120 125 Gln Ala Asn Ala Ala Phe Leu Val Gly Cys Tyr Met Val Ile Tyr Leu 130 135 140 Gly Arg Thr Pro Glu Glu Ala Tyr Arg Ile Leu Ile Phe Gly Glu Thr 145 150 155 160 Ser Tyr Ile Pro Phe Arg Asp Ala Ala Tyr Gly Ser Cys Asn Phe Tyr 165 170 175 Ile Thr Leu Leu Asp Cys Phe His Ala Val Lys Lys Ala Met Gln Tyr 180 185 190 Gly Phe Leu Asn Phe Asn Ser Phe Asn Leu Asp Glu Tyr Glu His Tyr 195 200 205 Glu Lys Ala Glu Asn Gly Asp Leu Asn Trp Ile Ile Pro Asp Arg Phe 210 215 220 Ile Ala Phe Cys Gly Pro His Ser Arg Ala Arg Leu Glu Ser Gly Tyr 225 230 235 240 His Gln His Ser Pro Glu Thr Tyr Ile Gln Tyr Phe Lys Asn His Asn 245 250 255 Val Thr Thr Ile Ile Arg Leu Asn Lys Arg Met Tyr Asp Ala Lys Arg 260 265 270 Phe Thr Asp Ala Gly Phe Asp His His Asp Leu Phe Phe Ala Asp Gly 275 280 285 Ser Thr Pro Thr Asp Ala Ile Val Lys Glu Phe Leu Asp Ile Cys Glu 290 295 300 Asn Ala Glu Gly Ala Ile Ala Val His Cys Lys Ala Gly Leu Gly Arg 305 310 315 320 Thr Gly Thr Leu Ile Ala Cys Tyr Ile Met Lys His Tyr Arg Met Thr 325 330 335 Ala Ala Glu Thr Ile Ala Trp Val Arg Ile Cys Arg Pro Gly Ser Val 340 345 350 Ile Gly Pro Gln Gln Gln Phe Leu Val Met Lys Gln Thr Asn Leu Trp 355 360 365 Leu Glu Gly Asp Tyr Phe Arg Gln Lys Leu Lys Gly Gln Glu Asn Gly 370 375 380 Gln His Arg Ala Ala Phe Ser Lys Leu Leu Ser Gly Val Asp Asp Ile 385 390 395 400 Ser Ile Asn Gly Val Glu Asn Gln Asp Gln Gln Glu Pro Glu Pro Tyr 405 410 415 Ser Asp Asp Asp Glu Ile Asn Gly Val Thr Gln Gly Asp Arg Leu Arg 420 425 430 Ala Leu Lys Ser Arg Arg Gln Ser Lys Thr Asn Ala Ile Pro Leu Thr 435 440 445 Leu Ser Ile Ser Arg Thr Lys Thr Val Leu Arg 450 455 <210> SEQ ID NO 806 <211> LENGTH: 3415 <212> TYPE: DNA <213> ORGANISM: Rattus norvegicus <400> SEQUENCE: 806 ctcgcgggac acagagagag aagcaccggt gcttgtgcct ggcgcctgcc gagtccccga 60 cgctcgcccg tccgcgccgc tgcccgtggc ggccgcgtct ctgaaccgcg gggtcgtgtt 120 tgtgtttgac ccgcgggcgc tggcgcgtgg cacgggctga agcgtgcagc ggggcggggg 180 ccggcgcacg gaggcggagg aagacgagcg ggagtccggg caggcccggc ggcgccatgg 240 aactgggccc ggagcccccc caccgccgcc gcctgctctt cacttgcagc cccactcctg 300 cgccgcagcc cacggggaag gtgcagtttg gcgcgtcacg tgctggcgga ctgtcccctg 360 tcaccaacct gacggtcacc atggaccagc tggaagggct gggcagtgac tatgagaaac 420 caatggacgt gagaaatagc agcagtctac agagaatggg ctcctctgaa tcgactgatt 480 caggtttctg tctagattct cctgggccct tggacagtaa agaaaacctt gaaatttccc 540 tgaggagaat aaattgccta cctcagaagc tcttggggtg tagcccagcg ctaaagagga 600 gccattctga ttctctagac cacgacatct ttcaactcat tgaccaggat gaaaataaag 660 aaaatgaagc atttgaattt aaaaagccaa taagacctgc atctcgtggc tgcctgaatg 720 ctcacgttca cgaggaaagt aaggacccct ttacacacag gcagaattca gccccagctc 780 ggatgctgtc ttcaaatgaa agtgacatta gtgaatcagg aaatttcagt cctcttttta 840 caccccagtc acctgtgaaa gcgagtttgt ctgatgagga tgatggcttc atagaccttc 900 tggatggaga gaatctgaag aatgatgagg agaccccgtc gtgcatgtca agcctctgga 960 ccgctcccct tgtcatgaga agacctacaa accttgccga tcgatgtgga ctgtttgact 1020 ccccttcccc gtgcagctcc accagcagct gcagcactcg ggcagtgaag agagcagacc 1080 gatctcatga ggagtctcct cgaggtacaa agcggaggaa gagcagtgag gccagtccag 1140 tgaaggcaga tgttccggag ccaacgcagc ttccacacca gtctctctcc ctgacatctt 1200 tccccaaagg aaccattgag aacattttcc acagtgaccc aagagacctt ataggggatt 1260 tctccaaggg ttacctcttt catacggtct ctgggaagca tcaggatttg aaatatattt 1320 ctccagaaat tatggcatct gttttgaatg gcaagtttgc caatctcatt aaagagtttg 1380 ttatcattga ctgccgatac ccatatgaat atgaaggagg gcacatcaag ggtgccgtga 1440 acttgcacat ggaagaagag gttgaggagt tcttactcaa gaaacctatc gtgcccgctg 1500 acggcaagcg tgtcattgtc gtgttccact gtgagttctc ctctgagaga ggccctcgga 1560 tgtgccgata tgtacgggaa cgagataggc ttggcaatga ataccccaaa ctccactacc 1620 ctgagctgta tgtcctgaag gggggataca aggagttctt tttgaaatgc cagtctcact 1680 gtgaaccccc cagctaccga ccgatgcacc atgaagactt taaagaagac ctaaagaagt 1740 tccgcaccaa gagccggacc tgggcagggg agaagagcaa aagggagatg tacagtcgcc 1800 tgaagaagct ttgaggccaa atggcagtga cctgagcttc cctccgccct gtccctttgt 1860 ccctttgctg tagagcagta agcaaagggg ccagctatac ggcacctgga ccctggagaa 1920 aaacctgggc cttccatgcc ttgaacctcc tacactccca ggttggagcc caggcatcct 1980 gccgtcacac tcttctgtga gagtccttcc ctgtcaggac tgtctgccaa agctggacaa 2040 gctcggcaca ggctggcaca ggctcgagtc tagtctggaa cgccacgtca ggctgctccg 2100 actaagcatc ccctgaagaa gtgcccaggc ctctcatgag gggagagaag ccactgaagt 2160 gctgctggcc aaataccaaa gataggctgg aaggggagag gtcctcatgg atgactcttt 2220 aatttattca gcctcatcaa ttattttatt attgttttaa ttcctcaaga cttttacttt 2280 actgcttcaa agtcaaaata ctgccattct aggtagagtt ttatcatcct aggaactacc 2340 tctactttta atttaaaaaa aaaacatggg gcagggataa gaaaaaaggc aaacctgtta 2400 agtgtgggca gcgcaaggaa ctcagtcacc cctaggaggc gctgtagact ggtattgctg 2460 ctattcaaag tcaaggactg agatgctggt cagagcctgc accaaccaga tccaggcttg 2520 gctacaggac ataagctaac cttcccagac ctacttctgc cctttgtgag ttcctttggg 2580 gagagtcttg tctgtactcc tggtcccagg tccccgtgac agtgactggt gtgggagttg 2640 caggaaggca catcaagcca cccccaggcc agtactggaa tgttgaagtg taccccaagg 2700 tgggagtggg gaggcatgga aaagtggagt ccacagagta agggaggagc atgcccactg 2760 aatgtccttt agaaaaaaaa aaaagtcatt ttatgagtca gagtatccaa tcagtgttgg 2820 gtgggcacct aagcttgagc agggggcggg aagcccgggc tgttacagac gactgtagaa 2880 tttctcagga gggcgtagta aattttgaag tcaaaagttc tgggtttcat catgttttaa 2940 ttgagggaca gagtggtgaa acacatcagt taccccctaa tctaaccccg tggaagtgag 3000 gctctgggga atgcctccca tctaaggagc tggcccgttt tgattctgtc agtgtcctcg 3060 ggcaccagcc tccctgccat ctgtgctcca ttggggtcat gccaggtttt tcttaggaag 3120 agtctcccct cttaacctct gctttctatt ctgggggtgg ggagggaatc aatgatattg 3180 aagatggcta gttgctttgt taagggtttg agtttgcatt tggctataaa acaaatcttg 3240 ttaaaaatat gtggagagca agggaatgag cagcctcttc ttcggtgtgt tgaagtatgt 3300 cctagttttc ccctggtctg gtttgtagag attctgttag ttgaatgcct tcaaggagaa 3360 tgaatggctt tcagattgta ccagcttagc tagcattgtt aaccagctgc tgcag 3415 <210> SEQ ID NO 807 <211> LENGTH: 525 <212> TYPE: PRT <213> ORGANISM: Rattus norvegicus <400> SEQUENCE: 807 Met Glu Leu Gly Pro Glu Pro Pro His Arg Arg Arg Leu Leu Phe Thr 1 5 10 15 Cys Ser Pro Thr Pro Ala Pro Gln Pro Thr Gly Lys Val Gln Phe Gly 20 25 30 Ala Ser Arg Ala Gly Gly Leu Ser Pro Val Thr Asn Leu Thr Val Thr 35 40 45 Met Asp Gln Leu Glu Gly Leu Gly Ser Asp Tyr Glu Lys Pro Met Asp 50 55 60 Val Arg Asn Ser Ser Ser Leu Gln Arg Met Gly Ser Ser Glu Ser Thr 65 70 75 80 Asp Ser Gly Phe Cys Leu Asp Ser Pro Gly Pro Leu Asp Ser Lys Glu 85 90 95 Asn Leu Glu Ile Ser Leu Arg Arg Ile Asn Cys Leu Pro Gln Lys Leu 100 105 110 Leu Gly Cys Ser Pro Ala Leu Lys Arg Ser His Ser Asp Ser Leu Asp 115 120 125 His Asp Ile Phe Gln Leu Ile Asp Gln Asp Glu Asn Lys Glu Asn Glu 130 135 140 Ala Phe Glu Phe Lys Lys Pro Ile Arg Pro Ala Ser Arg Gly Cys Leu 145 150 155 160 Asn Ala His Val His Glu Glu Ser Lys Asp Pro Phe Thr His Arg Gln 165 170 175 Asn Ser Ala Pro Ala Arg Met Leu Ser Ser Asn Glu Ser Asp Ile Ser 180 185 190 Glu Ser Gly Asn Phe Ser Pro Leu Phe Thr Pro Gln Ser Pro Val Lys 195 200 205 Ala Ser Leu Ser Asp Glu Asp Asp Gly Phe Ile Asp Leu Leu Asp Gly 210 215 220 Glu Asn Leu Lys Asn Asp Glu Glu Thr Pro Ser Cys Met Ser Ser Leu 225 230 235 240 Trp Thr Ala Pro Leu Val Met Arg Arg Pro Thr Asn Leu Ala Asp Arg 245 250 255 Cys Gly Leu Phe Asp Ser Pro Ser Pro Cys Ser Ser Thr Ser Ser Cys 260 265 270 Ser Thr Arg Ala Val Lys Arg Ala Asp Arg Ser His Glu Glu Ser Pro 275 280 285 Arg Gly Thr Lys Arg Arg Lys Ser Ser Glu Ala Ser Pro Val Lys Ala 290 295 300 Asp Val Pro Glu Pro Thr Gln Leu Pro His Gln Ser Leu Ser Leu Thr 305 310 315 320 Ser Phe Pro Lys Gly Thr Ile Glu Asn Ile Phe His Ser Asp Pro Arg 325 330 335 Asp Leu Ile Gly Asp Phe Ser Lys Gly Tyr Leu Phe His Thr Val Ser 340 345 350 Gly Lys His Gln Asp Leu Lys Tyr Ile Ser Pro Glu Ile Met Ala Ser 355 360 365 Val Leu Asn Gly Lys Phe Ala Asn Leu Ile Lys Glu Phe Val Ile Ile 370 375 380 Asp Cys Arg Tyr Pro Tyr Glu Tyr Glu Gly Gly His Ile Lys Gly Ala 385 390 395 400 Val Asn Leu His Met Glu Glu Glu Val Glu Glu Phe Leu Leu Lys Lys 405 410 415 Pro Ile Val Pro Ala Asp Gly Lys Arg Val Ile Val Val Phe His Cys 420 425 430 Glu Phe Ser Ser Glu Arg Gly Pro Arg Met Cys Arg Tyr Val Arg Glu 435 440 445 Arg Asp Arg Leu Gly Asn Glu Tyr Pro Lys Leu His Tyr Pro Glu Leu 450 455 460 Tyr Val Leu Lys Gly Gly Tyr Lys Glu Phe Phe Leu Lys Cys Gln Ser 465 470 475 480 His Cys Glu Pro Pro Ser Tyr Arg Pro Met His His Glu Asp Phe Lys 485 490 495 Glu Asp Leu Lys Lys Phe Arg Thr Lys Ser Arg Thr Trp Ala Gly Glu 500 505 510 Lys Ser Lys Arg Glu Met Tyr Ser Arg Leu Lys Lys Leu 515 520 525 <210> SEQ ID NO 808 <211> LENGTH: 31868 <212> TYPE: DNA <213> ORGANISM: Homo sapiens <400> SEQUENCE: 808 ccagggtctg tgagccctcc agagttgggc cctggtggtc gagtccagtc ctgggggtca 60 ttgcattccc tccctcatta taaaatgggg cctggaggcc cggggcggaa gaaaggggtc 120 cacaatactg cacggttaga ggccgagcca aggctggatc cggccagacc tccacaggtc 180 ttccttagcc tccacattgc ctcagagtgt ggggcgcccg gctgggggcg aggtagcgga 240 ggcccaaagg gggccgaagc taactggacg gcagctcgcg atgggaacta cgcttcccag 300 catgcgacgg ggcaaagggg cctttcagcc gcgagcagcg cctcgcaggt tctgctggga 360 gttttcattg acctctgctc cccctctcat tttgatcccc gctcttctgc tctgggctcc 420 gcccccttct gagagccgat gacctggcag agtcccgcga gccgctttct tcttcccctc 480 tcattggccc agcctagctg ccattcggtt gagaggagga gaagttgctt actgattggt 540 ggattccgtt tggcgccaac taggaaaggg gggcggggca gcagctggcc ccactgagcc 600 gctattaccg cgaaaggccg gcctggctgc gacagcctgg gtaagaggtg taggtcggct 660 tggttttctg ctacccggag ctgggcaagc gggtgggaga acagcgaaga cagcgtgagc 720 ctgggccgtt gcctcgaggc tctcgcccgg cttctcttgc cgacccgcca cgtttgtttg 780 gatttaatct tcaggttgcc ggcgcccgcc cgcccgctgg cctcgcggtg tgagagggaa 840 gcacccgtgc ctgtggctgg tggctggcgc ctggagggtc cgcacacccg cccggccgcg 900 ccgcttgccc gcggcagccg cgtccctgaa ccgcggagtc gtgtttgtgt ttgacccgcg 960 ggcgccggtg gcgcgcggcc gaggccggtg tcggcggggc ggggcggtcg cggcggaggc 1020 agaggaagag ggagcgggag ctctgcgagg ccgggcgccg ccatggaact gggcccggag 1080 cccccgcacc gccgccgcct gctcttcgcc tgcagccccc ctcccgcgtc gcagcccgtc 1140 gtgaaggcgc tatttggcgc ttcagccgcc gggggactgt cgcctgtcac caacctgacc 1200 gtcactatgg accagctgca gggtctgggc aggtaaggag agaccggcgg gcggtgctcc 1260 gggcccctgg cctcggtgtc ggcctcggag agatcaggcc aggaaacgga ccgggagaag 1320 ggcgagaccc gtccgtccgg gttcgccgct cggggacagc cgggctaggg cctgccatgt 1380 gcacccccgc ccgggcggaa tgttgggcgg gagaggccgt cgggaccttc caggggaaga 1440 ggtggagatc cttgggccta agcccgagcc aggcccacct tcaccccttt cggattgctc 1500 cgtactctcc ttctatctct atccctggaa gctctttgga atctaccccc gcggggaaaa 1560 tcaggctctt ctaggcactc actttcaccc tttgctaaac catcctcagg atcttcgttt 1620 gctgtgatct ttgttccttc tcaacaaagg accatggcat tttctttcct ggcgtttatg 1680 taaaatcatc tcagtccctc gccctgtgca cattcctgat gtccactctg ctgctttcct 1740 aaggccaggt ctttttaccc aactttcaga aagcttcctg ggcttttcct gatagcaaaa 1800 aatgcatccc acggtgtttc ccgcggaaga gctactttcc cttcaatctc tggcatcccg 1860 tttgctaagc acatgtcttg tgcgtttccc aacttctgaa aagcagaaag tgtcctgttc 1920 aactttcatc ccgactctgt ctcagtactt agaacacatg cttttatttt aggaaatacc 1980 ccaacatttg ccatagccat cataacctgc aatgtggtcc aaggccatgc ccacccactc 2040 cttttttctc ctttgcccaa gtgctaattg ggtgttcaga gtggcaaagt gggatctttg 2100 ccacttgtgg tgtggcctag aaatggtttc tggcagcctg gctgcttctt aatctcatgg 2160 cctatctcct gcatgtgacc ttttaattat atcctataaa tcattcatgg tttatttctg 2220 ttggtttcag tgattatgag caaccactgg aggtgaagaa caacagtaat ctgcagagaa 2280 tgggctcctc cgagtcaaca gattcaggta tttaagtctg ctgtgtgggg agcaatactc 2340 tgaatttcct gaaacatgcc ttttcaccca ggaggttagt tttggtgaga acttgaggaa 2400 gtcatggcat tgggtgataa actttttttt tttttttttt gagacagagt ttcgctcttg 2460 tcgcccaggc tggagtgcaa tggcatgatc tcagctcact gtaacctcca cctcccgggt 2520 tcaagtgatt ctcctgcctc agcctcccga gtagctggga ttacaggcat gcaccaccac 2580 acccggctaa ttttgtattt tttagtagag acagggtttc ttcatgttgg tcagcctggt 2640 ctcgaattca caacctcagg tgatccgcct tcctcggcct cccaaagtgc tgggattaca 2700 gcgtgagcca ccgcgcccgg tgataaacat tattgagaac aatacaaagg agcccttgtg 2760 gctgtttatg aagaaaggaa ataggtttca aatgtctata aggaggtggt gtgtgcttgc 2820 ccttgaagga tgggtagtaa agtataattc accataccac tgtaagtggc attcaggcaa 2880 tcttactggt taaaatacag gatcaaatga ttggaagtac agtgtcatga aatcatttca 2940 gtgatgctgc tatggaggaa attgccagtg catttcattc ttcatgaatt catattactg 3000 cagagtttat ctgtatttgt acagataaga ccattggtgc aaagatcctt taggttaaag 3060 gaactgcaag agcaagtctt aaaatgtaat gtaggcttct gtatgtagaa tgtaatttaa 3120 tatagaactg gggataggat tatcacttgt agcagtgtgg tgagcaaggg ctgtaacacc 3180 tcactttcca taaggctgta tagacacatg agctatgggt gggtgggtct gcgtcatctg 3240 agctggcata ttagtaatgc tgaacagtgt ctccttcacc ctgctgcctt ttgtgagatg 3300 gacaccttgg tgtcattttg ttaaaggcag caagtgcttg ccttgcatgt catgaccagt 3360 agttgtattt ttctttttca ttttgagaca aggtctcaac tctgtcaccc aggcaacctc 3420 tgcctcccag atttagagaa ttcttctgcc tcagcttccc tagtagctgg aattacaggt 3480 gtgggtctca aacttctgat ctcaggtgat ccacccactt cgacctccca aagtgctgag 3540 attacagggg tgagctactg cacctggcct tttttttttt ttttttttga gacagggtct 3600 tgctctgttt tccaggtctc aggctggtgt acagtggcac aatcagggtt cactgtagct 3660 tcaactttcc gagctcaagc gaacctccca ctccagcctc cccaagtagc tgggactaca 3720 gacacgtgcc accacaccca actaattttt tttttaactt tggtagagtc aagtctcact 3780 atgttgcccc aggcttgttt tgaacttgtg gcctcaagcc atcagcctgc ctcagcctcc 3840 caaagtattg gaatcacagg tgtgagccac tgtgcctggt cagtagttgt atttttcaag 3900 cctcatatga tttgacaagg taaaacgttt aaaaactatg ccaagaaaat ctggtaccta 3960 ttgtttctat ggttggaact cacagaaagt tatctgggtc acctctatct gaataaccaa 4020 acaatcatga tatgaatcag ttttattcac cctcttctca aatcctattt cccttgatgt 4080 tatttgcaaa taggagaaaa aacagtaaat acgctatgaa aatattaaga cttgtacaaa 4140 catgacattt ttgacaatct aatagacgta acatcaattc tggcaaaagt acaagccatg 4200 aatatttgtt gcctgactta aataaagacc caggtacttt gtttagtgtt ttaattttaa 4260 tgacaaaatg gtgttttttg tattatttct tgagaggttt tttttttccc cataggtttc 4320 tgtctagatt ctcctgggcc attggacagt aaagaaaagt atgtattcac tgctttcaaa 4380 tgtttatatg tagaaaaaac gtgtctaaac ttaaatacct tatttaaatg aagttcttca 4440 tacactggac tggagccctg gatttacctg tgcctagaaa cactctggaa tctcaagaat 4500 gaatagtttg tgtcagcaat tttcagaact ttttctcctt tattttagct ataattttgg 4560 tgttctgttt gggtcttacc caaaccctta ctctgtgctc tgacatcata gccttacaag 4620 aacatgtggg gtttttttgt ttgtttgttt gtttgtttct gaggcagagt ctcactctgc 4680 cgcccaggct agagtgcagt ggctcactgc aacctccacc tcccaggttc aactgattct 4740 cctgcctcag cctcccgagt agctgggact acaggagtgc accaccacac ccggttaatt 4800 tttgtatttt tagtagacac gaggtttcat cgtgttggcc aggccaggag ttcgagactc 4860 ctgagactcc tgacctcgtg atataccctc ctcggcctcc catagtgccc atagtgctgg 4920 gattacatgt gtgagccacc gcgcccagcc gaatgtgtgt attttaagaa aagacatggg 4980 tttgtttttt ttcacctaga agtctagtgt tgggggtgct cctgagaaca ggacagcttc 5040 agaaatttat tctcccatct cttgcctaaa atgggagtct gtgactgtac ccccaagcta 5100 caggctaaac actatctctc tgctaatatg aatacctctt tacttgtttt attctcatta 5160 tttaccttct gatctcatta cagccttgaa aatcctatga gaagaataca ttccctacct 5220 gtaagttagt tccttgttta ttttgagcta atacctgtta tctgttcctt agctaccagc 5280 atgaccttga taggagactt aatttagaga gtaaaaactg cttttcttta gtctcttttg 5340 agacaaggtc ttgctctgtc acccaggctg gagtgcagtg gcaaaatctt ggctcactgc 5400 aacctctgct tccctggctc aagtgatcct cccacctcaa cttccagagg agctgggact 5460 atatataggt gcacaccatc acacccggct gatttttgta ttttttgtag acatgggggt 5520 ctcactctgt tgcccaggct ggtttcaaac tcctgcctcg gcctcccaaa gtgctaggat 5580 tataggcaag agccactatt cccagccttt ccttagtctc ataagtactc aagatgttcg 5640 gtctggagga atttgtcctc catctctaac agagctttat taaaccagga agggttcttt 5700 tgatgcaaat gttatttggg gattgatttg gcactgtaat ccctgttgag gggggcactg 5760 tagaccttgt gaggttagct gtaaacccat ggaatggaaa cttctatgct gtgtcctggc 5820 tgtgtcctgg caaggtggat tcctggccac atttactggt tacctactgc agtgtgtgag 5880 gagctagtct accccctatt caacccccct tttttttctt ttgagaactg aattttccac 5940 tgaaatttta tttgtgtgcc ttaattattt tcctttttta ctttgatagc agaagctgtt 6000 gggatgtagt ccagctctga agaggagcca ttctgattct cttgaccatg acatctttca 6060 gctcatcgac ccagatgaga acaaggaaaa tgtgagtgtg acttcaatgt actaacctga 6120 ggcagaggtg aaacccacag gctgtcagtg gcttagaagt ggctgggctg ctttctggga 6180 gactaaactt ggccattatg tgcggtcttt ggagtcagag aattctgggt ttggatcctg 6240 cttactagct gtgtgatgtt ggcaaattct tctcttttta atctttgctc ttttgtaaaa 6300 taggagtagt aatacctttt agggatgttg tggcaataag taagattatg tatgaagtat 6360 tgaaaatggt gcctgacagg cgggagttgc tcagattgta gctcacagga gtaattacat 6420 gtacaaatag tgtttgtctg gaaggctctg cccaggctgt ccttgcctct ttgctctgac 6480 cctgaaatga attgtaagct taggaaaagg ctctttggca gtatttgtaa gaacggggtc 6540 aacaagttct agggaatctc agagtaactg aaatggtggc ttggaaggtg aatttctggt 6600 tatctaccct gaatgagcct ggcttttttg ttcttttaga cattgcacag agtaggcatc 6660 caaaacagtt gtaatttttt cagccttctc tctactgtat ttctatatat ttactttctc 6720 cccttttcca ttcctgctga aatgccacag ttcataatcc ttgtccttac aatcttcagg 6780 tttagtgtga aacccactgc ctccatgaac tctcctgatg atttctttat caacctggga 6840 agtgtcatga gaaagaatat ggaaatgagt tccagccttg agtgcttgga acagtgtatc 6900 agcctctagt gctttttacc agggcaaagc tgtactgatg cctggttttc ccccgaaata 6960 gcttctcagg gttgcttgcc tggagctttg ttttaaaggg aaaacagcat agatggtggt 7020 taaagagctc tcactctgga gttgtcctgt tttacttcaa tattttgggc acattcctta 7080 acctgcaagg tctagttttc tcacctgtaa aatcgggaca atcaggttgt atttgatggt 7140 taaaaagtta atgcacagaa agtacttagt actgtgttgg catagaaatc actgtaatat 7200 tagccattac tgcttttttt ttttttttga ttcttcatgg ttttatttct ctcagaactt 7260 taaaatgtga acattctata attcagccag tctttacttc caggtaactt ctttattggg 7320 tcgcaatacc cttttaaata acatgctctt gttccggaag gtagttagcc gttcatcact 7380 ctttctgtct aaataacatc cagtgacaaa tcccataggg acaagaacat gaacccagtg 7440 gtcccgcaca atctgaagta agttcaccat gatagctgca gcctcagtgc cgaccgcgac 7500 cccgagacca agggcaacgg ggaactcagc cacccacgcc agtgctagcc attactgctt 7560 ttaatactta attatgagtt cttaagtgaa tattttaggg caagggacct gtgagtgttt 7620 tcattccata aagtggaatc atacgatatg tattctatca tatctggctt taaaaaacat 7680 tatgcttgta agaatcgtcc acgttgagta aaccagtagg gctttttttt ttttcattgc 7740 ttttagtata gaatagaata attataagta gaaaaaatta tctccagttg gtaggaagag 7800 gtggaaaata tgaagccctg aaacagatgg acctagatgg aaaattttga caactattca 7860 caggcaatta tattagattt tatttatttt tgctttagat ttcagaaagt ttgtgattta 7920 gcttattcat cgtgttttgt atatttggca gatacttgtg ttaggaaata cagtatgaca 7980 agaaaaagat gttactttag aagttagctg ttgacagagc cttggaaatt cttagttacg 8040 cagatctatt gttggaatta ggtgaaactt taatttggag gcagaaaggt gatcagtgcc 8100 cactttcttg cctctttcac ccaagctgag gcctgagttg gttttcatgg acagtagatg 8160 tctcaactat gtcttgcagg aagcctttga gtttaagaag ccagtaagac ctgtatctcg 8220 tggctgcctg cactctcatg gactccagga gggtaaagat ctcttcacac agaggcagaa 8280 ctctgcccca gctcggatgg tatgtgctct ggctttcata ggggaattcc tgacaggaag 8340 aaaggattaa aacaccttct ttcatccaga attgaaggca ctacagtagc actagctgtt 8400 tttaccttga ctttgtcttt tgaaattaga ctgtcaagca ttcttggtgg ttttgctgtg 8460 tctggagaac agacaggcgg tagtaagagt gggagatggt gtttgaaata ttggagttgt 8520 gcaaggaata atcgaccttg ttaatctggg aaatcctggg tcatcctaaa tgtatgtatg 8580 gtgggattat atctcttcct atttttttct ttttttcttt tttttttttt aagggctttc 8640 tggcaaaaac cggaaagcct gcgagacaaa ttttaaaaga gccgtaacac tagatctctt 8700 acttaaaact tggtctttac tatgcattct aagtgcttct caaggaactg gagagagagc 8760 acttgacttc ttccaaaggt ggtttgttaa gaacagttat gggccaggtg ccatggctca 8820 tgcctataat ctcagcactt tggaaaactg agacaggagg atcgcttgag tcctgggcag 8880 catagtgaga ccacatctct atttttttta tttttaattt ttttaaagaa ctattatgga 8940 ttacagtgaa tgctcaggct gctgggcagt tttggggtca ctcgtttcag ggctatgtat 9000 ttgccagaca gggactgtca ttacttccaa agtttcctgc tgttggtctg aattggatta 9060 actgatagca tctatagatt ggagaggccc aacttgagca agatgaccac atttggcttc 9120 caggtttacc taggatctta aatctgaaaa tatacctttc caatctgctt tgtgttctga 9180 ggttcagcca gtattgttac tctgtctatc atttgcacaa agcactttta tatgttcttg 9240 tcttgtgaag tggagttaat ccacttgaac agattaggaa agtaccacta gagaggtttg 9300 gatgatttac caaaggatat acataagtag gaaaccagga tttaatgatc tctggctggg 9360 tgtggtggct catggctgta atcccagcac tttgggaggc cgaggtggga ggatcacatg 9420 aggtcaggag ttcaagacag cctgggtaac atagtgagac cctatctgta caaagttaaa 9480 aaataagctg agtgtggtgg cttgttccta tagtcccaat tagtcgggag gctgaagtgg 9540 gaggattgct tgagcccaag aattcgaggc tgcagtgagc tatgatcaga ccactgtact 9600 ccagcctgga caatgaatcc ctgtctcaat aaacaatctc taaattccca agtacacagt 9660 aatgctttaa gagttgggta tcagaaacaa tatatttggt gtgtgcttag cgactagagc 9720 ctgtatcaca tctgcaccta ggaatcccag aacatacctc acaaatgttg gtgtgatata 9780 gtgtgagctt tcgtgataaa ggtactgccc cataataaag ttatctaccc ctaggctaaa 9840 aaaatttgcc atttcccaga gtgtgcactt ggggaggact agagactgct cagaacttgt 9900 tttatattgt gaagcaaagc taatgccaga accagaatag gccagctgca gagaggattc 9960 cttggtgcat gatccactca gaaaatcaga gggccactta actaacaaca gattcatacc 10020 ccaaagagat ttggatttta aggattactt gtaggtcata acattgggac taccctgcta 10080 ctgtgaaaaa aataactcta aacttttttt tctggatttg aaagtgccta gaaaataaat 10140 aattcagtat tagcagtgtt tgtattggta ggatttatct tcaggtgtgg atttatgagc 10200 agtttttcta aattttctat attccatgtt tagaggtttc ccaaaaaaag tatgactata 10260 ggttggctaa tgaggtaccg ccattttaat tccaggaatg gttttctcct agggagatag 10320 tgtggtgaga agagtttgga ttttggagtc aaacagatga ggtgtataat cttggtaacc 10380 tcttaagcac cagtttcctg atttgctaaa gaaaaaggaa aggattagct acctttagtg 10440 tattgtgagg cttctattgg attatatgta taaagattat atcgtagtat ctggcacaca 10500 gtaattcctc gtttaaaaac tgagcattta aatcccaagt ctaaagaacg aggatagatt 10560 ttatagaagg aagttaccct ttattccccc ctgtcagaac tggagttata tataagtgca 10620 ttctctaggc cattttatgg tctttataga gatttgcatc tgcttgccct aactcatttc 10680 agcagattct catactgtca cagtcctcaa tgctgatcgg tgttcactga tgcaaccttc 10740 taataaaaga aaccttgttc ttcacaagag gctatctcta gtacccatta taaggtgaat 10800 tgcttctggc aagagttctc tgtaaaggct actgactact cagggctgtg tgtggtcatc 10860 aaatcattta taatcttggg atacattttc atataatcag taatggctaa aattttgctt 10920 tgtataacaa gtataacata gtatgttttc atcataaaaa ctagtgaccc attcaaggaa 10980 atgaaagtgg atcagagctc tcattattaa tccatgaatt ttgtcttaca gctttcctca 11040 aatgaaagag atagcagtga accagggaat ttcattcctc tttttacacc ccagtcacct 11100 gtgacagcca ctttgtctga tgaggatgat ggcttcgtgg accttctcga tggagagaat 11160 ctgaaggtac cgtgtgtgtg tgtgtgtgtt cctatttgtt ctactaatta attacctctg 11220 gagaaggcat gtgatgtgaa aaagaacagc aacagcagtt ccccggggct tgcttagctg 11280 atatttttgt tcatttggtg ataattcatt taataatagg gctaccagcc ttattaaatc 11340 ctttggattg ggggatgggg gcatcaaaag aagacacatg atccttctta ccctgaagga 11400 gctaactaac aatctatatg caagaaacat gaaatcagaa cggtatagga tggtacatta 11460 aggatacttc ctatccaggc ctatctggta ttgttcaggg agaaacacac ctaaagcact 11520 taaacaaatg ttagtctcta caggctcttt ttaaaatcag tttttctgtt tctttagaat 11580 gaggaggaga ccccctcgtg catggcaagc ctctggacag ctcctctcgt catgagaact 11640 acaaaccttg tgagttgttc tagtgtgtct ggaggaagcc ctgcgtgatt ggggcactgg 11700 acagagtagt ccttagttga gtatagccaa agattgaaat gcatgatagg atttggggat 11760 ctgggtttta ggcctcactt tggctaccta caaattatga cctttagtca tgatatctct 11820 ctgcatgtct cctgatgtat aaggagtgtg ggttaggagg gaccatggtc attcctagct 11880 tttaccatct agtcagtttg aaaaaagcct atctgaagcc tttagcctga atactttact 11940 ttttttaggt tattctcatt tatattccac agaacctagc ataaaattag acaagcaaca 12000 gtaactcaca ggattttttt tgtttctgtg ttttttgttt ttttttttga gacggagtct 12060 cgctcttgtt gcccattcta gagtgcagtg gcacaatctt ggctcactgc aacctctgcc 12120 tcccaggttc aagtgattct cctgcctcag cctcccgagt agctgggatt acaggtgcct 12180 gccaccacac ccagctaatc tttgtatttt cagtagagac ggggttacat tatgttggcc 12240 aggctagtct cgatctcctg acctcaggtg atctgcccac ctcgacctcc caaagtgctg 12300 ggattacagg catgagccac tgtgcctggc tggatgtttt ttgttgctgt tttgtttgtt 12360 tgttttgttt tgttttgttt ttcattgaaa atacctacct gaggctgggt attttcaggt 12420 agatattttc gattttaaaa attatatata atatatattt tatatatata tatatatata 12480 tatactcaca cacacacata cacagtatag atttgtgttt ccatcaggga tactttcaaa 12540 cagaaagcat agtatatgta gatacagaat ctatagtgta tgtgtgtata tatattcaaa 12600 atcacatata tatacacaca catacacatg ctatagattc gtgttttcat catagggata 12660 ctttcaaagt tagaagcaag aatgtgccta tacagatata tacacctgta tgttcagaga 12720 tatacaccct taggtacaca tctaaattga taagttcata ttttttaatt ctcaataacc 12780 tgaactataa ttacagaaca aatgagctac agtttttttg tttgtttgtt ttgttttgtt 12840 tttgagacag agtctccctc tgttgcccag gctggggtgc agtgcagtgg tgtagtcttg 12900 acttgctgca acctctgcct cctgggttca agtgcttctt ctggctcagc cttctgagta 12960 gctgggacta caggcttacg ccaccactcc cggctaattt ttttggtatt tttagtagag 13020 acgaggtttc actatgttgg ccaggctggt ctcgaactct tgacctcagg tgatccatcc 13080 acctgcctcc caaagtgctg ggattacagg catgagccac cgtgcccagc caagctacag 13140 ttttgagatc acttatggat tatagtacat tcatgtgcat agcttttgag aaaatatgtt 13200 aacgcagtac aaatgttatg agtaaattta ccaggtcatt ttgataggca taaaattaca 13260 taaaatgtga gaacactttg gaagtggctg ttagttttat agatttgatt ttagagtcat 13320 aagcatgggc ttgtaagctc ttaatagtgg ggaaatgtct tccacaaatg gttattacaa 13380 actaaccatt gctgggagct gtaatggaaa ataaacttca cacaaaagag gaagaaaatc 13440 cccggtctct atgggagcag atgtgggagt gatccattct actggggact atcaggaaga 13500 tttcaaagaa gtgacattga aatgttagca tcaacttgaa aatgaatggt ttactgagat 13560 gtgaaaggac attctgtgca gaaggaaaag ccaggccaag acacatggag tcgagaatag 13620 gctgagatgc gtttagagag ctgactcttg ctaccactgg tcagattggc ttcccttggg 13680 ctctggaaaa tttgtcttta tttatttatt tatttattga gacagagtct tgctctgtca 13740 cccaggctgg agtgcagtgg tgcaaatctt agctcactgc aaccaccacc tcctggtttc 13800 aagtgattct cgtgcctcag cctcctgggt agctgggatt aaaggcacgc accaccacac 13860 ctggctaatt tttttgtatt tttaatagag atggggtttc ttcatgttgg ccaggctgtt 13920 attgaacttg tgacctcaag tgatcccaca gtgttgggat tacaggcgtg agccaccgcg 13980 cccagcctgg gaaattagtc tttaaaagac caagtagaaa aaaagacttt gaacacaatt 14040 ttgaaaggca tttgctactc tgcccatccc cactccctcc aaatttacca tcttaactat 14100 accttaacca aagatgcccc catttttatt ataacctggc tactgtgcat cttttctgga 14160 tttaagtggg gtatttaaac ccgttgacct gcttaattaa gcaaggtgca agtaataaaa 14220 tggaggggaa gataggcaag ccaaaaatgt gttcctgact ggaaggtcac acttctcttg 14280 acgcaggatt atgtagacag tttttgtgag ggcaaaggac gttttgctca tctctatata 14340 atgtcagctg agtatatatt cattgagcac taagtgctca gtgcctacta tgtgccaggc 14400 cctgtgagag ttgctaggac tagatgaatc ggcagtgtct gttggctaat ttagaattga 14460 tcttagatca tcccaggaaa ccttcggttt atttgtctta ccattcaagt gaacaggttt 14520 taatgaaaga tgggtctgtc tgtttttttt cctgtaagga caaccgatgc aagctgtttg 14580 actccccttc cctgtgtagc tccagcactc ggtcagtgtt gaagagacca gaacgatctc 14640 aagaggagtc tccacctgga agtacaaaga ggaggaagag catgtctggg gccagcccca 14700 aagagtcaac taatccagag aaggcccatg aggttagttt cctaggttcc tttttgctct 14760 agcacagata ctgtattttt cagttctaaa aatttctact tagtggttca tttattttct 14820 ttgctaagat ttgctggggt tttgtggggt tgtgtgtgtg tgtgggtgtg tgtgtgtttc 14880 ttttaataga gatgggatct agcgatgttg cccacgctgg tcctgaactc ctagcctcaa 14940 gtgatcctcc tgccttggcc tcccaaagca ctgggattac aagtgtgagc caccacacct 15000 ggctgatact tggctgtttt catgttggtt tttcatttgc tttgagtatg ttcataattg 15060 cctgttgaag catttttaag atggctgctt taaaatcttt gtaagacaaa tccaacatcc 15120 atccatagtg ttgttggcat ctgttgattg tcttttcctg ttcaagttgg gatttttctg 15180 gttcttggta tgaccggtga ttcttccatt gtctcctgta tatttgtgag tctccggtct 15240 atgtaaattt tacgttttag caggcttcct ctgatactgc aagaaaggca tgggtggaag 15300 tccgggttcc ccagcacaaa ctccattgac accttgggtg gggacttgtc tcattattgc 15360 tgggagggag tggaagttca ttccatcccc gtggggtggt gactggggca ctgtatgaca 15420 gctgggcaaa ggtggaggcc cccgcttgct gttggccata attgtttctg tgttgactag 15480 tagaatgatt attgtctaaa agtcttctgc ctcaataggc catcctttgc ctagggagag 15540 caggcttttc ttggggcttg ttgtgttgct gtctccagct tcatgagttg aatggttaac 15600 tcattcgttt ttaattttct tatttctgga taaatctatt tgaatctatg aatttcccac 15660 tgctttagat ttgtctcata acttttgacc tgaaatgttt ttattatcat ttgttgtaga 15720 tattttattt ccttttaatc cagacctatc atggcctatt aaatacttga tttttataaa 15780 ggtctgtctt tttttttttt ttttttgaga cgctctgtcg cccaggctgg agtgcagtgg 15840 cgcgatctca gctcactgca agctctgcct cccgggttca tgccattctc ctgcttcagc 15900 ctcccagtag ctgggactac aggaccccgc caccacgcct ggctaatttt ttgtattttt 15960 agtagagacg gggtttcaca gtgttagcta ggatggtctc catctcctga ccttgtgatc 16020 cgcccgcctc agcctcctaa agtgctggaa ttacaggcgt gagccactgc gcccagccct 16080 gtctgtctaa ttcttcaagt taattcattg cattgctcat agttgtatag gctgttttgt 16140 tgtttcctgt ttctgagaca gggtctctct gtcacccagg ctggagtgca gtggcatgat 16200 ctccgctcac tgcactctcc acctcccagg ctcaagcagt cctcccacct caggctctca 16260 agcagctggg actataggtg tgtgccacca aacccagcta atttttgtat tttttgtaga 16320 gacaggcttt cgccatgttg cgcaggctgg tctcaaactc ctgggctcag ggcaatcctc 16380 ccgccttggc ctcccaaagt gccaggatca taggtgttag acacagcacc tggcatgggt 16440 gagctagtgt catggttgtc tgggcctaag tcctatggtc ctttgtgtta ttttttctat 16500 ttattctgtg gctagacaca caaaacactg gtttatttgt atgtttttcc ttcattatac 16560 tgtccttata ttgaggtttg gtattaagca ttataaaatg gtgaactacc tgtgttttct 16620 gtggcatgaa aaggtttaag taaatctcat cacagtctta aaaggttaga gagatgacag 16680 ctaggaaaac atttagcatt taggcctact gccttatcgt atctgctttt gtttttaatg 16740 ctttatgaat gtttttaaag tattgttcta aaagaatatt ttaataattg catagtattt 16800 ttgttttggg agagttgttt ggttttggtt tttgttcttt ttgtttgtgg ggggcacagg 16860 gtctagcgct gtcactcagg ctggagtgca ctagcacgat cacagctcag tacagcctcc 16920 atgggctcaa gcactcctcc cgcctcagcc cccctagcag ctgggactac aggcatgcac 16980 caccatgccc agttaattta aaaaaaattt ttttttattt tttgtagaaa agaggtctta 17040 ctgtgttgcc caggctggcc ttgaattcct gggctcaagc agtcctccca cctcagcctc 17100 caaagtatct gggactacag gcacaggcca gtgcacctgg ccgatagtgt tttgacttac 17160 aagtatacta gaaataattg aataaatcac cttctggaca tttagaattt cccttcccct 17220 gattttcctt ttatttctaa ttaaaaatga aattctgggt tataagggca agaacatttg 17280 tgaaacttta cattgtatac atgtcagaaa atatctatca atatttaata atattctggc 17340 tgagtgctgt ggttcactcc tgtaatccca gcactttggg aggacaaggc gggtggatca 17400 cgaggtcagg agttccatac cagcctggcc aatatggtga aaccctgtct ctactgaaaa 17460 tacaaaaaat agctgggtgt ggtggtatga gcctgtaatc ccagctgctc aggaggctga 17520 ggcaggagaa tcgcttgaac ccgggaaatg gaggttgcag tgagcagaga tcacgccact 17580 gcactccagc ctgggtgata gagtgagatt tcatctcaaa aaaaaaaaaa aaagaatatt 17640 cattttcttt ttctttcttt ttgagacacg ctggagtgca gtggcaggat cttggctcac 17700 ggcaacctcc gcctccccag ttcaagcaag tctctgcctc agcctcctga gtagctggga 17760 ttacaggtgc ccactgccac gcctggctaa ttttttttgt atttttagta gaggcggagt 17820 ttcaccaagt tggccaggct ggtcttgaac tcctgacctc aggtgatata tccgccttgg 17880 cctcccaaag tgctggggtt acaggtgtga gccactgtgc ccggccagaa tattcatttt 17940 cttttaccgt aatagagatt gaccttttta tttccatatt tgtaaaactt tttttggata 18000 aaataatact gttaataatt attttgtata tatattggcc ctcatgtttt ggtttatttt 18060 catatatttt aatttttagt attttaaatt ccattgtgga gaaaatgtca agcattgcta 18120 gagtacagtt atcatacctg tgatattgtg aaatatatat ttagtcttct tccccttctg 18180 tcatataact cctaaaatct ttggaatatc caaggtcata tctttttgta tactaatgat 18240 tgatagcttc agggtgggac tggtcactgg aaagacagag acatgattag aggttggaac 18300 tttcagcccc accctccaat gtctacggaa aggagagggg ctaaaggtca agttgatcac 18360 tcatggccaa tggtttaatc aatcatttct atgtaatgaa gcctccctaa aaccttgaaa 18420 ggacagggtt cagagagctt ctggatagct gaacacatgg aggttcctgg aggttggggc 18480 acccaaggag agcatggcag ctccatgtcc cttctcccat acctcaccct atgcatgtct 18540 tcttctatat cctttgaata tccttcataa taaactggta aatgtgtttt cttgagttct 18600 gtgagccact tctagcaaat taaacccaaa gaaggggtca tgggaacccc tacttaaagc 18660 tggtggtcgt agatcagaag atccagaggc ccaactggtg tctgaagggt ggtgtggttt 18720 tgaggactgg gccctcaact tcctgatctg acgctctgca ggtagatagt gtcagaattg 18780 aattggacgg cacccagcta ttttccactg cagaactgct tgcttgcttg cttgcttgct 18840 ggtagggaga aatcccctca tatctggggg taacagcact tctgtcttct gttgctgttg 18900 agtgagggaa taagaaaaat cactttgagt ttgtggggtg ttttcctcac acaaacatat 18960 catacagggc taaatttctg ggtgtttttt tgtttgtttt tttttttgag accaagtctc 19020 gctctgtcgc ccagactgga gtgccatggg tcgatctctg ctcactgcaa cctccgcctc 19080 tcaggttcca gcaattctcc cgcctcagcc tcccaagtag ctgggactac aggcgcccac 19140 caccacgcct ggctaatttt ttatattttt agtagagacg gggtttcacc atgttggcaa 19200 ggctggtctc gaacccctga catcaagtga tccactcacc tcggcctccc aaagtgctgg 19260 gattacaggc atgagccacc acgcccggca gagctaaatt tcttactatc aaatgtcaaa 19320 tatccagtct gggttcagtt ttccccagtt gtctcctaag tacttttaca gtttatttgt 19380 taaaatctgg atccaaataa agtctataca ctgtagttgg tcaataggtc tcttactctt 19440 cagatttcag tgctccatct gtttccctct tgcatatttt tatttgttga agagctcaag 19500 tcatttgtcc tgcaaaggtt cccacagtcc tgtggggtct tcagacattg tcttctatcc 19560 cctatattgc cttaacctaa ctctggaaag gatggattga attccagttc tatttgtttg 19620 gcaagaatat cacataggtg attttgtcta ctttgatcag gaagtataat gtgccaggca 19680 gccattggtg attgctgccc agatttttta cttcatttca ccagggtttc agaaagatga 19740 tactgcagtt tttacattct ttcctcatta attagctaga atatatctat aaagagaaac 19800 ttacactcat caaacactgt ggttaccctt gggaaaggca ggatgaatat tggatctctt 19860 tatttgccag tttccaaata atgccctacc aagcatcttc caaagttgaa agcaagactt 19920 atagttgttt ttcaataata atcaggaatt catgggttaa aacatttaat gtgtttctgt 19980 gtattacaag tattatcctt ttactcaaat tatccccttt ttaacagctg gcttcctctt 20040 ctcattgaat aaagctaaga cgtaggccgg gcgcggtggc tcacacctgt aatcccagca 20100 ctttgggagg ccaaggcagg cagatcacct gaggccagga gttcaagacc atctggccaa 20160 catggtgaaa ccccgtctct actaaaaata caaaaattag ctgggcgtgg tggcgcacac 20220 ctatagtctc agctgctctg gaggctgcgg cagaatcgct tgaacctggg aggcagaggt 20280 tacagtgagc caagatcact gtactccagc ctgcactcca ctcctgtact ccactgcact 20340 ccagcctgag cgacagagcg agactctgtc tttttaaaaa aaaaaaaaaa aaaaagttaa 20400 gacatacttt ttctaaactt aatcctagtt ttaacccccc ttgtttcttt ctctttttct 20460 ggagatagtt tcagtctgtc acccaggctg gagtgcagtg gcaccatcac cacttgctgt 20520 agcctcgacc tccccaggct caggtgatcc tcccacttca gcctcccaag tagctgggac 20580 tacaggcaca caccaccatg cccagcttgt gtgtgtgtgt gtgtgtgtgt gtgtgtgtgt 20640 gtgtgtgtgt gtgtgtggac agggtcttgc tctttgatct ggtctggaac tcctgggctc 20700 aagcgattca cctgccttgc ccaggctggt ctggaactcc tgggctcaag tgagtaaccc 20760 accttggcct cccaaagtgc tgggattaca ggcatgagcc aaaccacctg cacccccttt 20820 tttttttttt ttttttaagg aaggaaggaa aacttagttt cagagcaatt cggttagaca 20880 ctggaataat aggagaccta gtcaataacc cacatctgtt tttgttcact ccagattcaa 20940 taaaataaaa taaaaacttc ttactaaatg taggcattaa cattttagtc tcctcgagac 21000 atgctccaag tgaatgtttt cagaagttcc attcagaacc cttgtctcat tctctacctt 21060 tgatttgtta cagactcttc atcagtcttt atccctggca tcttccccca aaggaaccat 21120 tgagaacatt ttggacaatg acccaaggga ccttatagga gacttctcca aggtaattgc 21180 aagcagagct gctctggcaa gtgtaggagg gagtgtgggt atttagaatc ccactcagcc 21240 tgtctccctc cccagggtgg ttcctggcat acctccaaaa ggacacagtt aaaagaatgt 21300 taaaggtagg gaagcaaact tagtttctca tgatcaggta tatgttggtt tctgagactg 21360 tagatatcac tatagctgat gggcagtttt aggtagggag ctgtccacca accaccttga 21420 ttgtaaccca aagactaggc tctctgggaa ctgtgttatt ataaaaatag taattagcag 21480 gatagtgtac agcagaaata aatctgtagc cacactacaa gtctgcatgt tgaaaggtta 21540 tcttagaagg tctgggattg agactgaatt tctccgttca gagaagcttg gccattgagg 21600 gaaaagaccc tccaggaagt ctagaggaag atcttctaat agcctgatat actacatgaa 21660 ggcttggctg cagtaaaata caaggctagg acagggaatg tgtcaatagc agcttcttta 21720 atcacatttt gacttgaagg ttaccagatc aatgttttat tcattaattt agttaacatt 21780 tattgaagca cttatgtgtt aggcagagat tccaaaatga gatacagttc cttccctcaa 21840 agaatttagc atgtggttgg agaggtgaga cgtgaactac atgtaccaca tggtagactg 21900 aaataaattt tagtgaggtg taaacataaa cagcatgccg tgagaagtaa aagggtttat 21960 cttggctagg gggttgggga acgtctgggg ttgggccgtt gatatttcag cccaaatggg 22020 ttttgaagga acggagaatg aagagaacaa gcaaagatcc agctgtatcc tcagttttgg 22080 aaccttctct tgtttggcag ggagagatgt ggtcttacta tgttgctcag gctgtagtgc 22140 agtggctatt cgcacatgct atcatagtac actgtagcct caaacttatg gcctcaagtg 22200 ctccccctgc ctcagcctcc caagtagctg ggactacagg catgcaccac cacactcagt 22260 ggaattttca acttgaattg aggcctggtt atatttgtct taatgggcct atgcatgggg 22320 atagatgaac tcttggctca gccagtcacc ctaatgagta attgctaatg tgtgcatctt 22380 cctcctcaag gctgggctag gtctcttttt ttcctatccc cagtgcctgg caccatgctg 22440 gacatagcag gtgctcagta aatgagtgaa atctgtatgt ttaagtgcta ttcgcagtct 22500 aactactgac gtgtggattc ttgacaaaag caggaggaaa atgagattac ctgaggtttc 22560 tttatttaaa tctgccttac tagctaggta accttggata aggtgctcaa aatggggata 22620 atatacctca ttggtttgtg tgaaaattaa atgtcaggat gttaatgaag taactagaag 22680 agtaactagt gtgtactaac taatgtttgt ttgcttgttt gtttgtttgt tttttgagag 22740 ggagtcttgc tctgtcaccc aggctggagt gcagtggtgc aatctcagct cactgcaacc 22800 tccgcctcct gtgattcaag cgattttccc actccagcct tccgagtagc tgggactata 22860 ggtgcatgct aacgcccggc taatttttgt atttttaaaa gagttggggt ttcaccatgt 22920 tggccaggct tgtctcgaac tcctgacctc aggtgatcca ctagcctcgg cctcccaaag 22980 tgctgggatt acaggtgtga gccaccgtgc ctggccatta atgtttgttt tttaaaagat 23040 gcctcctacc agccagacaa aacagtataa gtgtgaataa tatataggct ttcagattct 23100 ctaagtatct ttttttcttt ttaagggtta tctctttcat acagttgctg ggaaacatca 23160 ggatttaaaa tacatctctc cagaaattgt aagtccatcc ttttgaaacc caccacacat 23220 cgggtacttg aatctagttt tccctgacgg tcaaagttga ttctccctaa ttttctctca 23280 acagatggca tctgttttga atggcaagtt tgccaacctc attaaagagt ttgttatcat 23340 cgactgtcga tacccatatg aatacgaggg aggccacatc aaggtatgga ttcctgagac 23400 ttgctgtaga aggagcccta aacaggatct gtggttttaa agtggggagg acagtgacac 23460 ctggccactt agctcatatg ctagttgtta gaattttgaa acaatacagt gagtgtggaa 23520 ggcatttgat tccgggtgct cttaacgaat gttcccttgt ctgcaatact ctctaccacc 23580 ttgtgctaca gttattcttc atgtttgtcc ctcacaccat cattatcaag gacacttgta 23640 ggaggtaccc actgatgttt aagtcattcg ggggacaaga atgggtttca tagcatttaa 23700 gaggcttggg taccaatgtc tgagcacccc agggctcctg atgaggagaa gaccatctct 23760 ggcaacatgt cctggtgtct gtgccaggct tagtgatgcc tccaaagttg attgttcagc 23820 aagctgcctg gtggaggggc gtgttgggac acacgttccc aagaagaaag gaactgattt 23880 tgccatttta atcttttttt tttttttttt tttgagacag agtccgctct gtcgccaggc 23940 tggagtgcag tggcatgatc tcggatcacc acaacctctg cctcctgggt tcaagcaatt 24000 ctcctgcctc agccttccaa gtagctggga ctacaggtgc acgctgccac gcccggctaa 24060 tttttttttt tttttagtag agacggggtt tcaccatgtt gcccgggctg gtctcaaact 24120 cctgagctca ggcaaaccgc ccgcctcagc ctcccaaagt gctaggatta caggcatgag 24180 ccacggcgcc tggcctgcca ttttaatgtt ttacccgatt aatagtgttt aaatatagta 24240 aggaggtact ttaaatacga tgttactgtt tgccattgtc ttgtggcttt tgaaaatccc 24300 caaatttata aaactaccta taaagtgtac cattgtcata tttgaattgc ccatttccag 24360 tccccatgtg cattactgta tgatgaacgt gtacggaccc acaaagctcc attgagatac 24420 aggtgccaaa tggtctactg ggctattcag ctagaagaac tgcaaaaatc acaaactggt 24480 cttgtggact taaagatcac tcttgatgaa tcattacatc ttgctgaatc attacttcat 24540 gtgtgaaacg tgcaggttcc aagggtctct gttgtcttca cagggtgcag tgaacttgca 24600 catggaagaa gaggttgaag acttcttatt gaagaagccc attgtaccta ctgatggcaa 24660 gcgtgtcatt gttgtgtttc actgcgagtt ttcttctgag agaggtcccc gcatgtgagt 24720 gctgcacgga actgggttct ggggcacagg ctccatgatg cttttgtggg acatggtggt 24780 ttgtggcttg cacttggagc atattttagc atatcaagca acctctggca cataacaagc 24840 cattttcata tgtaatttta tcctgaggtg aactttggct cttccagtct ccccgactgt 24900 ccttagtctg atctgtgggg ctactgttct catgtgacct ccttcaagta caaagtgacc 24960 gttccttatg caaatgccag aaaagtgtga agttctcatt ctgtaaaacc tcatatgata 25020 tgatgctttg aaacacttga tattattacc aatttcaggg tgaaaagaaa aaagggggcc 25080 aaagagctgc ccatcagtca tctgtgtcca ttctaaaagg attgcaagcc tgctgtttgt 25140 caggcactga caataaaaat gtaactacag taaaacacag tacagtaaaa ataccacagc 25200 gagcaggacc aacaaggacc ctactgcagc agagatccaa gtggggatcc gtataaatgc 25260 taggaggaca ggcagagagg taggacagag agtgcagctt aactaggatg gtccaaggga 25320 gacttctgca ggaccacgtt cttatgccac ctttttattt tgaaccaatt tattttaaaa 25380 aacattttta aattaaaaaa tttcaatttt ttttttttga cggagttttg ctcttgttgc 25440 ccaggctgga gtgcagtggc acaatctctt ctcactgcaa cctctgcctc ccaggttcaa 25500 gcagttctcc tgcctcagcc tcccaagtag ctgggattac aggcatgcgc catcacgccc 25560 ggctaatttt gtatttttag tagaggcagg gtttctacat gttggtcagg ctggtcttga 25620 actcccgacc ttaggtgatc cgcctgcctc agcctcccaa agtagtggga ttacaggcgt 25680 gagccactgc acctggcttt ttctttcttt ctttctttct tttttttttt tttttttgag 25740 gcagaggcac actgttttca cccagactgg aatgcagtgg catgatctcg gctcactgca 25800 acctccacct cctgggttca agcgattctc ctgcctcagc ctcctgagta gctgggataa 25860 caggcgtgca ccaccacacc cggctaattt ttgtatttgt agtagagatg ggggtttcac 25920 catgttggcc gggctggtct tgaactcctg acctcaggtg atccacccgc cttgacctcc 25980 caaagtgctg ggattacagg tgtgagccac cacgcccagc agaaatttca aattttgaga 26040 tggggtctta atatattggc caggttggtc tcaaactcct ggcctcaagc aatcctctct 26100 ccttggcctc caaagtgcta ggattgcagg catgagccac tgtgcccacc cctttgaacc 26160 tttttttttt tttgagacgg agtctcgctc tgtcacccag gctggagtgc agtggcacaa 26220 tctcgactta ctgcaagctc cgcctcctgg gttcatgcca ttctcctgcc tcagcctccc 26280 gagtagctgg gactacaggt gcccaccatc acgcctggct aatttttttg tatttttagt 26340 agagacaggg tttcaccatt ttagccagga tggtctccat ctcctgacct tgcgatctgc 26400 ccgtctcggc ctcccaaagt gcttggatta caggcgtgag ccactgcgcc tgacctgaac 26460 cattttaaag ctcaagaaga ggtgaggtta tggctgggca cagtggcacc tgtaatccca 26520 acactttggg aggccgaggc aggaggatca cttgctcggg agtttcagac cagaccaacc 26580 tgggtaacac agtgggacca cacctctaca aaaaatagga ggtgggagga tcgtttgagc 26640 ccagcaggtc gaggctgtgg tgagccatga tcatgccact gtactccagc ctaggtgaca 26700 gagtgagatt ctgtctctct ctcacacaca cacacacaca cacacacaca cacacaaagg 26760 ttatacttgc acacacttca cctgatttta ttaattttta acattttgtc acatttgtat 26820 gtacatgctc tacacacagg caactacagt acaacttgac acttttgact gtcatctcat 26880 aagtccttca aacatctgtc tccaaaggat gctcattcat gaatggaatt attcactcag 26940 cagttttttt gtttgtttgt ttgagatgta gtcttgctct gccacccaga ctggagtgca 27000 gtggtgcgat ctcggatcac tgcaacctcc acctcccggg ttcaagcaat tctcctgcct 27060 caggctccca agtagctggg actacgggtg catgccacca tgccaagcta atgtttgtat 27120 ttttagtaga gacggggttt tgctacattg gccaggctgg tctcgaactc ctgacctcaa 27180 gtgatctacc cgcctcagcc tcccaaagtg ctgggattat aggcctgaaa caaactaatc 27240 tggacacaca tacacacaca tgtaaattgt ttttaaaccc acaaaagatg ctgctctctt 27300 ttttttttat ttttgagtca gggtcagtct ctgttgtcca ggctggagta cagtggcagg 27360 agcacagctc actgtagcct ctgcctccca ggctcaagtg attctcccac ctcagcctcc 27420 caggaagcta ggaccacaaa catgcatcac catgcctggc taatttttgt attttttata 27480 gagacagggt ctcactgtgt tgcccaggct ggtctcaaac tcctgggctc aggcaatcct 27540 ggcctcccaa agtgcttgga ttacaggtgt gagccgccat gcccagccca aaagatgcta 27600 ttctcttaat ctctcatttc cccatcttcc tctttaacac ctctaatata aaggacatta 27660 ttataccata ttgaaacttc acctagatat acagaaaacg ccccatctct gtattctgta 27720 tttgcaagct gcatgtttat atcaccatct acagataccc cttacacttc gttccccact 27780 tgagtttcgc catcactggc tttctgttgt tccactgggg aaagatttgg gattcacagg 27840 tgaactcttt tttttttttt tttttttttt tgagttggaa tctcgccctt tcgcccaggc 27900 tggaatgcag tggcacaatc tcggctcact gcagcctcct cctcccgggt tcaagcattt 27960 ctctgcctca gcctcccaag tagctgggat tacaggcacc tgccaccacg cccagctaat 28020 tttttgtagt tttagtagac acagggtttc actatcttgg ccaggctggt ctcgaactcc 28080 tgacctcgtg atccaccgcc tcagcctccc aaagtgctgg aattacaggt gtgagccacc 28140 gcgcccagcc aaactccttt taaccacagg caaatggttt aagctacgtg ctgcagagga 28200 agctgctgcc catccctcat gagcagctaa caaaggcccc aaaccactga gcttcaagag 28260 aaaatcagca gatactcttg gctcttgtgt accagatacc tttctagata ctgagggaga 28320 agagcagtga acaaaacaga ccaaaaaatc tctgccttca tggaacttac atttcggagt 28380 ggacaggaga tcgagaccag cctggccaac atggtgaaat cccgtctcta ctaaaaatac 28440 aaaaattagc caggcgtggt ggcggacacc tgtaatccca gctactttgg aggctgaggc 28500 aggagcatcc cttgaaccca ggaggcagag gttgcagtga gccgagatcg cgccagtgca 28560 ctccagcctg ggcgacagag tgagactcca tctcaaaaaa aaaaaaaaaa aggtgactgg 28620 gtgcggtggc taactcctgt aatcccaaca ctttgggagg ccaaggcagg tggatcacaa 28680 ggtcaagagg tcgagaccat cctggccaac atggtgaagc cccatctcta ctaaacatac 28740 aaaaatcagc tgggcggtgg cacgcgcctg tagtcccagc tatttgggag gctgaggcag 28800 gagaattgct tgaacccggg agacggagat tgcagtgagc ctgaggtcac gcccttgcac 28860 tccagcctgg tgacagagtg agattctgtc tcagaaaaaa gaaggtgctt cagaggaaaa 28920 taaggccagt ggtggagctc ccaggcaggc tggaggaaca gtagtggggc tgcaggggct 28980 ggcgtggggt gaacaagggg cagagcagca gtaggggcct gtagagctgt aggcctctga 29040 aggacttggg gcctcgggct ttttcaccaa gggcgaggca gtaagcagcc attggctgga 29100 tattgaagac cattcagtcc aagtagagga tagaaacagg gccccgaggc aggagcaagt 29160 tcagcctctt taaaagccac agaaagaaac aagcccactt atgtagaagg aggtgagtga 29220 gggagcctgg ctgaagagaa ggctggggtg gagaaagcaa ggggaagctg gctcatatag 29280 tgaaaacttg ccacaaactg tggtggtgaa ggtgctgggc aggactcaga tgctaggatt 29340 gttggagaaa ggaaaattgg ggaagagacc atctactggc actggctgtg agtgctgctc 29400 atgtggccag gaacttgcaa ctcagcactg attgtttcta agaataaatg tcaagttggg 29460 aagatgtgta taagggggac ttagaccaca actgctgctt tgactgcgtt gccttgttgc 29520 tgtgctggaa aagctaaccc tgctttggcc ttccttcccc tgactaggtg ccggtatgtg 29580 agagagagag atcgcctggg taatgaatac cccaaactcc actaccctga gctgtatgtc 29640 ctgaaggggg gatacaagga gttctttatg aaatgccagg taagactggg gttgtggaga 29700 gcatctctcc tcccctgccc ccagtggtag actaatggat ctgtctggtg gtcatgactt 29760 tctttccagg ggtcggggga caaggtgggt atctgctgaa cccaaagaaa gcccctgtag 29820 aactggctcc ctaggtctgc ctggccgctt tcagccttgt agccctaggc agagaggaaa 29880 ccaggttgtg ggtgtgaggc aggtgtaccc taaccttatt ctctcctgtc ccctcagtct 29940 tactgtgagc cccctagcta ccggcccatg caccacgagg actttaaaga agacctgaag 30000 aagttccgca ccaagagccg gacctgggca ggggagaaga gcaagaggga gatgtacagt 30060 cgtctgaaga agctctgagg gcggcaggac cagccagcag cagcccaagc ttccctccat 30120 ccccctttac cctctttgct gcagagaaac ttaagcaaag gggacagctg tgtgacattt 30180 ggagaggggg cctgggactt ccatgcctta aacctacctc ccacactccc aaggttggag 30240 cccagggcat cttgctggct acgcctcttc tgtccctgtt agacgtcctc cgtccatatc 30300 agaactgtgc cacaatgcag ttctgagcac cgtgtcaagc tgctctgagc cacagtggga 30360 tgaaccagcc ggggccttat cgggctccag ccatctcatg aggggagagg agacggaggg 30420 gagtagagaa gttacacaga aatgctgctg gccaaatagc aaagacaacc tgggaaggaa 30480 aggtctttgt gggataatcc atatgtttaa tttattcaac ttcatcaatc actttatttt 30540 attttttttt ctaactcctg gagacttatt ttactgcttc attaggttga aatactgcca 30600 ttctaggtag ggttttatta tcccagggac tacctcggct tttaatttaa aaaaaaaaaa 30660 gaagtgggta agaaaatgca aacctgttat aagttatcgg acagaaagct aggtgctctg 30720 tcacccccag gaggcgctgt ggtactgggg ctgctgctat ttaagccaag aactgaggtc 30780 ctggtgagag cgttggaccc aggcttggct gcctgacata agctaaatct cccagaccca 30840 ccactggcta ccgatatcta tttggtggga ggtgtggccc tgttcttcct caccccagtt 30900 ccatgacatt ggctggtata ggagccacag tcaggaaagc acttgaggca gcatctgttg 30960 ggccaccccc ggctcagtgc tggaatgttg cagtgtaggt ttcccaggga aggggggtgg 31020 gggtaggtgg gctccacagg atgggggagg agcatgtcca ctgagtatct tccttatgtt 31080 gctgtgatat tgatagcttt tattttctaa tttttaaaaa atggtcatat tatgagtcaa 31140 agagtatcaa atcagtgttg gatggaccac ccaagggtga ggagaggggc tggaagccct 31200 gggcattagg agaagggagt gggtgctggc atggacatga ctggatagaa ttttctcagg 31260 agggagcttg gtggattttg aaggtaaaac tttctgggtt tatcatgttt taattttaga 31320 gacagggagt gatgaatcat caccggttgt ccccttatct aactccataa aagtgggaat 31380 ttcaaaagaa cacctcatcc aaggagctgg ggcagacttc attgattcta gagagacctg 31440 tttcagtgcc tactcatccc tgccctctgg tgccagcctc cttaccatca cggcttcact 31500 gaggtgtagg tgggtttttc ttaaacagga gacagtctct cccctcttac ctcaacttct 31560 tggggtggga atcagtgata ctggagatgg ctagttgctg tgttacgggt ttgagttaca 31620 tttggctata aaacaatctt gttgggaaaa atgtggggga gaggacttct tcctacacgc 31680 gcattgagac agattccaac tggttaatga tattgtttgt aagaaagaga ttctgttggt 31740 tgactgccta aagagaaagg tgggatggcc ttcagattat accagcttag ctagcattac 31800 taaccaactg ttggaagctc tgaaaataaa agatcttgaa cccatgctct ctgcctagtt 31860 cttgatgg 31868 <210> SEQ ID NO 809 <211> LENGTH: 524 <212> TYPE: PRT <213> ORGANISM: Homo sapiens <400> SEQUENCE: 809 Met Glu Leu Gly Pro Glu Pro Pro His Arg Arg Arg Leu Leu Phe Ala 1 5 10 15 Cys Ser Pro Pro Pro Ala Ser Gln Pro Val Val Lys Ala Leu Phe Gly 20 25 30 Ala Ser Ala Ala Gly Gly Leu Ser Pro Val Thr Asn Leu Thr Val Thr 35 40 45 Met Asp Gln Leu Gln Gly Leu Gly Ser Asp Tyr Glu Gln Pro Leu Glu 50 55 60 Val Lys Asn Asn Ser Asn Leu Gln Arg Met Gly Ser Ser Glu Ser Thr 65 70 75 80 Asp Ser Gly Phe Cys Leu Asp Ser Pro Gly Pro Leu Asp Ser Lys Glu 85 90 95 Asn Leu Glu Asn Pro Met Arg Arg Ile His Ser Leu Pro Gln Lys Leu 100 105 110 Leu Gly Cys Ser Pro Ala Leu Lys Arg Ser His Ser Asp Ser Leu Asp 115 120 125 His Asp Ile Phe Gln Leu Ile Asp Pro Asp Glu Asn Lys Glu Asn Glu 130 135 140 Ala Phe Glu Phe Lys Lys Pro Val Arg Pro Val Ser Arg Gly Cys Leu 145 150 155 160 His Ser His Gly Leu Gln Glu Gly Lys Asp Leu Phe Thr Gln Arg Gln 165 170 175 Asn Ser Ala Pro Ala Arg Met Leu Ser Ser Asn Glu Arg Asp Ser Ser 180 185 190 Glu Pro Gly Asn Phe Ile Pro Leu Phe Thr Pro Gln Ser Pro Val Thr 195 200 205 Ala Thr Leu Ser Asp Glu Asp Asp Gly Phe Val Asp Leu Leu Asp Gly 210 215 220 Glu Asn Leu Lys Asn Glu Glu Glu Thr Pro Ser Cys Met Ala Ser Leu 225 230 235 240 Trp Thr Ala Pro Leu Val Met Arg Thr Thr Asn Leu Asp Asn Arg Cys 245 250 255 Lys Leu Phe Asp Ser Pro Ser Leu Cys Ser Ser Ser Thr Arg Ser Val 260 265 270 Leu Lys Arg Pro Glu Arg Ser Gln Glu Glu Ser Pro Pro Gly Ser Thr 275 280 285 Lys Arg Arg Lys Ser Met Ser Gly Ala Ser Pro Lys Glu Ser Thr Asn 290 295 300 Pro Glu Lys Ala His Glu Thr Leu His Gln Ser Leu Ser Leu Ala Ser 305 310 315 320 Ser Pro Lys Gly Thr Ile Glu Asn Ile Leu Asp Asn Asp Pro Arg Asp 325 330 335 Leu Ile Gly Asp Phe Ser Lys Gly Tyr Leu Phe His Thr Val Ala Gly 340 345 350 Lys His Gln Asp Leu Lys Tyr Ile Ser Pro Glu Ile Met Ala Ser Val 355 360 365 Leu Asn Gly Lys Phe Ala Asn Leu Ile Lys Glu Phe Val Ile Ile Asp 370 375 380 Cys Arg Tyr Pro Tyr Glu Tyr Glu Gly Gly His Ile Lys Gly Ala Val 385 390 395 400 Asn Leu His Met Glu Glu Glu Val Glu Asp Phe Leu Leu Lys Lys Pro 405 410 415 Ile Val Pro Thr Asp Gly Lys Arg Val Ile Val Val Phe His Cys Glu 420 425 430 Phe Ser Ser Glu Arg Gly Pro Arg Met Cys Arg Tyr Val Arg Glu Arg 435 440 445 Asp Arg Leu Gly Asn Glu Tyr Pro Lys Leu His Tyr Pro Glu Leu Tyr 450 455 460 Val Leu Lys Gly Gly Tyr Lys Glu Phe Phe Met Lys Cys Gln Ser Tyr 465 470 475 480 Cys Glu Pro Pro Ser Tyr Arg Pro Met His His Glu Asp Phe Lys Glu 485 490 495 Asp Leu Lys Lys Phe Arg Thr Lys Ser Arg Thr Trp Ala Gly Glu Lys 500 505 510 Ser Lys Arg Glu Met Tyr Ser Arg Leu Lys Lys Leu 515 520 <210> SEQ ID NO 810 <211> LENGTH: 2940 <212> TYPE: DNA <213> ORGANISM: Homo sapiens <400> SEQUENCE: 810 gccagctgtg ccggcgtttg ttggctgccc tgcgcccggc cctccagcca gccttctgcc 60 ggccccgccg cgatggaggt gccccagccg gagcccgcgc caggctcggc tctcagtcca 120 gcaggcgtgt gcggtggcgc ccagcgtccg ggccacctcc cgggcctcct gctgggatct 180 catggcctcc tggggtcccc ggtgcgggcg gccgcttcct cgccggtcac caccctcacc 240 cagaccatgc acgacctcgc cgggctcggc agccgcagcc gcctgacgca cctatccctg 300 tctcgacggg catccgaatc ctccctgtcg tctgaatcct ccgaatcttc tgatgcaggt 360 ctctgcatgg attcccccag ccctatggac ccccacatgg cggagcagac gtttgaacag 420 gccatccagg cagccagccg gatcattcga aacgagcagt ttgccatcag acgcttccag 480 tctatgccgg tgaggctgct gggccacagc cccgtgcttc ggaacatcac caactcccag 540 gcgcccgacg gccggaggaa gagcgaggcg ggcagtggag ctgccagcag ctctggggaa 600 gacaaggaga atgatggatt tgtcttcaag atgccatgga agcccacaca tcccagctcc 660 acccatgctc tggcagagtg ggccagccgc agggaagcct ttgcccagag acccagctcg 720 gcccccgacc tgatgtgtct cagtcctgac cggaagatgg aagtggagga gctcagcccc 780 ctggccctag gtcgcttctc tctgacccct gcagaggggg atactgagga agatgatgga 840 tttgtggaca tcctagagag tgacttaaag gatgatgatg cagttccccc aggcatggag 900 agtctcatta gtgccccact ggtcaagacc ttggaaaagg aagaggaaaa ggacctcgtc 960 atgtacagca agtgccagcg gctcttccgc tctccgtcca tgccctgcag cgtgatccgg 1020 cccatcctca agaggctgga gcggccccag gacagggaca cgcccgtgca gaataagcgg 1080 aggcggagcg tgacccctcc tgaggagcag caggaggctg aggaacctaa agcccgcgtc 1140 ctccgctcaa aatcactgtg tcacgatgag atcgagaacc tcctggacag tgaccaccga 1200 gagctgattg gagattactc taaggccttc ctcctacaga cagtagacgg aaagcaccaa 1260 gacctcaagt acatctcacc agaaacgatg gtggccctat tgacgggcaa gttcagcaac 1320 atcgtggata agtttgtgat tgtagactgc agatacccct atgaatatga aggcgggcac 1380 atcaagactg cggtgaactt gcccctggaa cgcgacgccg agagcttcct actgaagagc 1440 cccatcgcgc cctgtagcct ggacaagaga gtcatcctca ttttccactg tgaattctca 1500 tctgagcgtg ggccccgcat gtgccgtttc atcagggaac gagaccgtgc tgtcaacgac 1560 taccccagcc tctactaccc tgagatgtat atcctgaaag gcggctacaa ggagttcttc 1620 cctcagcacc cgaacttctg tgaaccccag gactaccggc ccatgaacca cgaggccttc 1680 aaggatgagc taaagacctt ccgcctcaag actcgcagct gggctgggga gcggagccgg 1740 cgggagctct gtagccggct gcaggaccag tgaggggcct gcgccagtcc tgctacctcc 1800 cttgcctttc gaggcctgaa gccagctgcc ctatgggcct gccgggctga gggcctgctg 1860 gaggcctcag gtgctgtcca tgggaaagat ggtgtggtgt cctgcctgtc tgccccagcc 1920 cagattcccc tgtgtcatcc catcattttc catatcctgg tgccccccac ccctggaaga 1980 gcccagtctg ttgagttagt taagttgggt taataccagc ttaaaggcag tattttgtgt 2040 cctccaggag cttcttgttt ccttgttagg gttaaccctt catcttcctg tgtcctgaaa 2100 cgctcctttg tgtgtgtgtc agctgaggct ggggagagcc gtggtccctg aggatgggtc 2160 agagctaaac tccttcctgg cctgagagtc agctctctgc cctgtgtact tcccgggcca 2220 gggctgcccc taatctctgt aggaaccgtg gtatgtctgc catgttgccc ctttctcttt 2280 tcccctttcc tgtcccacca tacgagcacc tccagcctga acagaagctc ttactctttc 2340 ctatttcagt gttacctgtg tgcttggtct gtttgacttt acgcccatct caggacactt 2400 ccgtagactg tttaggttcc cctgtcaaat atcagttacc cactcggtcc cagttttgtt 2460 gccccagaaa gggatgttat tatccttggg ggctcccagg gcaagggtta aggcctgaat 2520 catgagcctg ctggaagccc agcccctact gctgtgaacc ctggggcctg actgctcaga 2580 acttgctgct gtcttgttgc ggatggatgg aaggttggat ggatgggtgg atggccgtgg 2640 atggccgtgg atgcgcagtg ccttgcatac ccaaaccagg tgggagcgtt ttgttgagca 2700 tgacacctgc agcaggaata tatgtgtgcc tatttgtgtg gacaaaaata tttacactta 2760 gggtttggag ctattcaaga ggaaatgtca cagaagcagc taaaccaagg actgagcacc 2820 ctctggattc tgaatctcaa gatgggggca gggctgtgct tgaaggccct gctgagtcat 2880 ctgttagggc cttggttcaa taaagcactg agcaagttga gaaaaaaaaa aaaaaaaaaa 2940 <210> SEQ ID NO 811 <211> LENGTH: 566 <212> TYPE: PRT <213> ORGANISM: Homo sapiens <400> SEQUENCE: 811 Met Glu Val Pro Gln Pro Glu Pro Ala Pro Gly Ser Ala Leu Ser Pro 1 5 10 15 Ala Gly Val Cys Gly Gly Ala Gln Arg Pro Gly His Leu Pro Gly Leu 20 25 30 Leu Leu Gly Ser His Gly Leu Leu Gly Ser Pro Val Arg Ala Ala Ala 35 40 45 Ser Ser Pro Val Thr Thr Leu Thr Gln Thr Met His Asp Leu Ala Gly 50 55 60 Leu Gly Ser Arg Ser Arg Leu Thr His Leu Ser Leu Ser Arg Arg Ala 65 70 75 80 Ser Glu Ser Ser Leu Ser Ser Glu Ser Ser Glu Ser Ser Asp Ala Gly 85 90 95 Leu Cys Met Asp Ser Pro Ser Pro Met Asp Pro His Met Ala Glu Gln 100 105 110 Thr Phe Glu Gln Ala Ile Gln Ala Ala Ser Arg Ile Ile Arg Asn Glu 115 120 125 Gln Phe Ala Ile Arg Arg Phe Gln Ser Met Pro Val Arg Leu Leu Gly 130 135 140 His Ser Pro Val Leu Arg Asn Ile Thr Asn Ser Gln Ala Pro Asp Gly 145 150 155 160 Arg Arg Lys Ser Glu Ala Gly Ser Gly Ala Ala Ser Ser Ser Gly Glu 165 170 175 Asp Lys Glu Asn Asp Gly Phe Val Phe Lys Met Pro Trp Lys Pro Thr 180 185 190 His Pro Ser Ser Thr His Ala Leu Ala Glu Trp Ala Ser Arg Arg Glu 195 200 205 Ala Phe Ala Gln Arg Pro Ser Ser Ala Pro Asp Leu Met Cys Leu Ser 210 215 220 Pro Asp Arg Lys Met Glu Val Glu Glu Leu Ser Pro Leu Ala Leu Gly 225 230 235 240 Arg Phe Ser Leu Thr Pro Ala Glu Gly Asp Thr Glu Glu Asp Asp Gly 245 250 255 Phe Val Asp Ile Leu Glu Ser Asp Leu Lys Asp Asp Asp Ala Val Pro 260 265 270 Pro Gly Met Glu Ser Leu Ile Ser Ala Pro Leu Val Lys Thr Leu Glu 275 280 285 Lys Glu Glu Glu Lys Asp Leu Val Met Tyr Ser Lys Cys Gln Arg Leu 290 295 300 Phe Arg Ser Pro Ser Met Pro Cys Ser Val Ile Arg Pro Ile Leu Lys 305 310 315 320 Arg Leu Glu Arg Pro Gln Asp Arg Asp Thr Pro Val Gln Asn Lys Arg 325 330 335 Arg Arg Ser Val Thr Pro Pro Glu Glu Gln Gln Glu Ala Glu Glu Pro 340 345 350 Lys Ala Arg Val Leu Arg Ser Lys Ser Leu Cys His Asp Glu Ile Glu 355 360 365 Asn Leu Leu Asp Ser Asp His Arg Glu Leu Ile Gly Asp Tyr Ser Lys 370 375 380 Ala Phe Leu Leu Gln Thr Val Asp Gly Lys His Gln Asp Leu Lys Tyr 385 390 395 400 Ile Ser Pro Glu Thr Met Val Ala Leu Leu Thr Gly Lys Phe Ser Asn 405 410 415 Ile Val Asp Lys Phe Val Ile Val Asp Cys Arg Tyr Pro Tyr Glu Tyr 420 425 430 Glu Gly Gly His Ile Lys Thr Ala Val Asn Leu Pro Leu Glu Arg Asp 435 440 445 Ala Glu Ser Phe Leu Leu Lys Ser Pro Ile Ala Pro Cys Ser Leu Asp 450 455 460 Lys Arg Val Ile Leu Ile Phe His Cys Glu Phe Ser Ser Glu Arg Gly 465 470 475 480 Pro Arg Met Cys Arg Phe Ile Arg Glu Arg Asp Arg Ala Val Asn Asp 485 490 495 Tyr Pro Ser Leu Tyr Tyr Pro Glu Met Tyr Ile Leu Lys Gly Gly Tyr 500 505 510 Lys Glu Phe Phe Pro Gln His Pro Asn Phe Cys Glu Pro Gln Asp Tyr 515 520 525 Arg Pro Met Asn His Glu Ala Phe Lys Asp Glu Leu Lys Thr Phe Arg 530 535 540 Leu Lys Thr Arg Ser Trp Ala Gly Glu Arg Ser Arg Arg Glu Leu Cys 545 550 555 560 Ser Arg Leu Gln Asp Gln 565 <210> SEQ ID NO 812 <211> LENGTH: 2115 <212> TYPE: DNA <213> ORGANISM: Homo sapiens <400> SEQUENCE: 812 ggtcaacgcc tgcggctgtt gatattcttg ctcagaggcc gtaactttgg ccttctgctc 60 agggaagact ctgagtccga cgttggccta cccagtcgga aggcagagct gcaatctagt 120 taactacctc ctttccccta gatttccttt cattctgctc aagtcttcgc ctgtgtccga 180 tccctatcta ctttctctcc tcttgtagca agcctcagac tccaggcttg agctaggttt 240 tgtttttctc ctggtgagaa ttcgaagacc atgtctacgg aactcttctc atccacaaga 300 gaggaaggaa gctctggctc aggacccagt tttaggtcta atcaaaggaa aatgttaaac 360 ctgctcctgg agagagacac ttcctttacc gtctgtccag atgtccctag aactccagtg 420 ggcaaatttc ttggtgattc tgcaaaccta agcattttgt ctggaggaac cccaaaatgt 480 tgcctcgatc tttcgaatct tagcagtggg gagataactg ccactcagct taccacttct 540 gcagaccttg atgaaactgg tcacctggat tcttcaggac ttcaggaagt gcatttagct 600 gggatgaatc atgaccagca cctaatgaaa tgtagcccag cacagcttct ttgtagcact 660 ccgaatggtt tggaccgtgg ccatagaaag agagatgcaa tgtgtagttc atctgcaaat 720 aaagaaaatg acaatggaaa cttggtggac agtgaaatga aatatttggg cagtcccatt 780 actactgttc caaaattgga taaaaatcca aacctaggag aagaccaggc agaagagatt 840 tcagatgaat taatggagtt ttccctgaaa gatcaagaag caaaggtgag cagaagtggc 900 ctatatcgct ccccgtcgat gccagagaac ttgaacaggc caagactgaa gcaggtggaa 960 aaattcaagg acaacacaat accagataaa gttaaaaaaa agtatttttc tggccaagga 1020 aagctcagga agggcttatg tttaaagaag acagtctctc tgtgtgacat tactatcact 1080 cagatgctgg aggaagattc taaccagggg cacctgattg gtgatttttc caaggtatgt 1140 gcgctgccaa ccgtgtcagg gaaacaccaa gatctgaagt atgtcaaccc agaaacagtg 1200 gctgccttac tgtcggggaa gttccagggt ctgattgaga agttttatgt cattgattgt 1260 cgctatccat atgagtatct gggaggacac atccagggag ccttaaactt atatagtcag 1320 gaagaactgt ttaacttctt tctgaagaag cccatcgtcc ctttggacac ccagaagaga 1380 ataatcatcg tgttccactg tgaattctcc tcagagaggg gcccccgaat gtgccgctgt 1440 ctgcgtgaag aggacaggtc tctgaaccag tatcctgcat tgtactaccc agagctatat 1500 atccttaaag gcggctacag agacttcttt ccagaatata tggaactgtg tgaaccacag 1560 agctactgcc ctatgcatca tcaggaccac aagactgagt tgctgaggtg tcgaagccag 1620 agcaaagtgc aggaagggga gcggcagctg cgggagcaga ttgcccttct ggtgaaggac 1680 atgagcccat gataacattc cagccactgg ctgctaacaa gtcaccaaaa agacactgca 1740 gaaaccctga gcagaaagag gccttctgga tggccaaacc caagattatt aaaagatgtc 1800 tctgcaaacc aacaggctac caacttgtat ccaggcctgg gaatggatta ggtttcagca 1860 gagctgaaag ctggtggcag agtcctggag ctggctctat aaggcagcct tgagttgcat 1920 agagatttgt attggttcag ggaactctgg cattcctttt cccaactcct catgtcttct 1980 cacaagccag ccaactcttt ctctctgggc ttcgggctat gcaagagcgt tgtctacctt 2040 ctttctttgt attttccttc tttgtttccc cctctttctt ttttaaaaat ggaaaaataa 2100 acactacaga atgag 2115 <210> SEQ ID NO 813 <211> LENGTH: 473 <212> TYPE: PRT <213> ORGANISM: Homo sapiens <400> SEQUENCE: 813 Met Ser Thr Glu Leu Phe Ser Ser Thr Arg Glu Glu Gly Ser Ser Gly 1 5 10 15 Ser Gly Pro Ser Phe Arg Ser Asn Gln Arg Lys Met Leu Asn Leu Leu 20 25 30 Leu Glu Arg Asp Thr Ser Phe Thr Val Cys Pro Asp Val Pro Arg Thr 35 40 45 Pro Val Gly Lys Phe Leu Gly Asp Ser Ala Asn Leu Ser Ile Leu Ser 50 55 60 Gly Gly Thr Pro Lys Cys Cys Leu Asp Leu Ser Asn Leu Ser Ser Gly 65 70 75 80 Glu Ile Thr Ala Thr Gln Leu Thr Thr Ser Ala Asp Leu Asp Glu Thr 85 90 95 Gly His Leu Asp Ser Ser Gly Leu Gln Glu Val His Leu Ala Gly Met 100 105 110 Asn His Asp Gln His Leu Met Lys Cys Ser Pro Ala Gln Leu Leu Cys 115 120 125 Ser Thr Pro Asn Gly Leu Asp Arg Gly His Arg Lys Arg Asp Ala Met 130 135 140 Cys Ser Ser Ser Ala Asn Lys Glu Asn Asp Asn Gly Asn Leu Val Asp 145 150 155 160 Ser Glu Met Lys Tyr Leu Gly Ser Pro Ile Thr Thr Val Pro Lys Leu 165 170 175 Asp Lys Asn Pro Asn Leu Gly Glu Asp Gln Ala Glu Glu Ile Ser Asp 180 185 190 Glu Leu Met Glu Phe Ser Leu Lys Asp Gln Glu Ala Lys Val Ser Arg 195 200 205 Ser Gly Leu Tyr Arg Ser Pro Ser Met Pro Glu Asn Leu Asn Arg Pro 210 215 220 Arg Leu Lys Gln Val Glu Lys Phe Lys Asp Asn Thr Ile Pro Asp Lys 225 230 235 240 Val Lys Lys Lys Tyr Phe Ser Gly Gln Gly Lys Leu Arg Lys Gly Leu 245 250 255 Cys Leu Lys Lys Thr Val Ser Leu Cys Asp Ile Thr Ile Thr Gln Met 260 265 270 Leu Glu Glu Asp Ser Asn Gln Gly His Leu Ile Gly Asp Phe Ser Lys 275 280 285 Val Cys Ala Leu Pro Thr Val Ser Gly Lys His Gln Asp Leu Lys Tyr 290 295 300 Val Asn Pro Glu Thr Val Ala Ala Leu Leu Ser Gly Lys Phe Gln Gly 305 310 315 320 Leu Ile Glu Lys Phe Tyr Val Ile Asp Cys Arg Tyr Pro Tyr Glu Tyr 325 330 335 Leu Gly Gly His Ile Gln Gly Ala Leu Asn Leu Tyr Ser Gln Glu Glu 340 345 350 Leu Phe Asn Phe Phe Leu Lys Lys Pro Ile Val Pro Leu Asp Thr Gln 355 360 365 Lys Arg Ile Ile Ile Val Phe His Cys Glu Phe Ser Ser Glu Arg Gly 370 375 380 Pro Arg Met Cys Arg Cys Leu Arg Glu Glu Asp Arg Ser Leu Asn Gln 385 390 395 400 Tyr Pro Ala Leu Tyr Tyr Pro Glu Leu Tyr Ile Leu Lys Gly Gly Tyr 405 410 415 Arg Asp Phe Phe Pro Glu Tyr Met Glu Leu Cys Glu Pro Gln Ser Tyr 420 425 430 Cys Pro Met His His Gln Asp His Lys Thr Glu Leu Leu Arg Cys Arg 435 440 445 Ser Gln Ser Lys Val Gln Glu Gly Glu Arg Gln Leu Arg Glu Gln Ile 450 455 460 Ala Leu Leu Val Lys Asp Met Ser Pro 465 470 <210> SEQ ID NO 814 <211> LENGTH: 1896 <212> TYPE: DNA <213> ORGANISM: Homo sapiens <400> SEQUENCE: 814 ggtcaacgcc tgcggctgtt gatattcttg ctcagaggcc gtaactttgg ccttctgctc 60 agggaagact ctgagtccga cgttggccta cccagtcgga aggcagagct gcaatctagt 120 taactacctc ctttccccta gatttccttt cattctgctc aagtcttcgc ctgtgtccga 180 tccctatcta ctttctctcc tcttgtagca agcctcagac tccaggcttg agctaggttt 240 tgtttttctc ctggtgagaa ttcgaagacc atgtctacgg aactcttctc atccacaaga 300 gaggaaggaa gctctggctc aggacccagt tttaggtcta atcaaaggaa aatgttaaac 360 ctgctcctgg agagagacac ttcctttacc gtctgtccag atgtccctag aactccagtg 420 ggcaaatttc ttggtgattc tgcaaaccta agcattttgt ctgggtcacc tggattcttc 480 aggacttcag gaagtgcatt tagctgggat gacaatggaa acttggtgga cagtgaaatg 540 aaatatttgg gcagtcccat tactactgtt ccaaaattgg ataaaaatcc aaacctagga 600 gaagaccagg cagaagagat ttcagatgaa ttaatggagt tttccctgaa agatcaagaa 660 gcaaaggtga gcagaagtgg cctatatcgc tccccgtcga tgccagagaa cttgaacagg 720 ccaagactga agcaggtgga aaaattcaag gacaacacaa taccagataa agttaaaaaa 780 aagtattttt ctggccaagg aaagctcagg aagggcttat gtttaaagaa gacagtctct 840 ctgtgtgaca ttactatcac tcagatgctg gaggaagatt ctaaccaggg gcacctgatt 900 ggtgattttt ccaaggtatg tgcgctgcca accgtgtcag ggaaacacca agatctgaag 960 tatgtcaacc cagaaacagt ggctgcctta ctgtcgggga agttccaggg tctgattgag 1020 aagttttatg tcattgattg tcgctatcca tatgagtatc tgggaggaca catccaggga 1080 gccttaaact tatatagtca ggaagaactg tttaacttct ttctgaagaa gcccatcgtc 1140 cctttggaca cccagaagag aataatcatc gtgttccact gtgaattctc ctcagagagg 1200 ggcccccgaa tgtgccgctg tctgcgtgaa gaggacaggt ctctgaacca gtatcctgca 1260 ttgtactacc cagagctata tatccttaaa ggcggctaca gagacttctt tccagaatat 1320 atggaactgt gtgaaccaca gagctactgc cctatgcatc atcaggacca caagactgag 1380 ttgctgaggt gtcgaagcca gagcaaagtg caggaagggg agcggcagct gcgggagcag 1440 attgcccttc tggtgaagga catgagccca tgataacatt ccagccactg gctgctaaca 1500 agtcaccaaa aagacactgc agaaaccctg agcagaaaga ggccttctgg atggccaaac 1560 ccaagattat taaaagatgt ctctgcaaac caacaggcta ccaacttgta tccaggcctg 1620 ggaatggatt aggtttcagc agagctgaaa gctggtggca gagtcctgga gctggctcta 1680 taaggcagcc ttgagttgca tagagatttg tattggttca gggaactctg gcattccttt 1740 tcccaactcc tcatgtcttc tcacaagcca gccaactctt tctctctggg cttcgggcta 1800 tgcaagagcg ttgtctacct tctttctttg tattttcctt ctttgtttcc ccctctttct 1860 tttttaaaaa tggaaaaata aacactacag aatgag 1896 <210> SEQ ID NO 815 <211> LENGTH: 400 <212> TYPE: PRT <213> ORGANISM: Homo sapiens <400> SEQUENCE: 815 Met Ser Thr Glu Leu Phe Ser Ser Thr Arg Glu Glu Gly Ser Ser Gly 1 5 10 15 Ser Gly Pro Ser Phe Arg Ser Asn Gln Arg Lys Met Leu Asn Leu Leu 20 25 30 Leu Glu Arg Asp Thr Ser Phe Thr Val Cys Pro Asp Val Pro Arg Thr 35 40 45 Pro Val Gly Lys Phe Leu Gly Asp Ser Ala Asn Leu Ser Ile Leu Ser 50 55 60 Gly Ser Pro Gly Phe Phe Arg Thr Ser Gly Ser Ala Phe Ser Trp Asp 65 70 75 80 Asp Asn Gly Asn Leu Val Asp Ser Glu Met Lys Tyr Leu Gly Ser Pro 85 90 95 Ile Thr Thr Val Pro Lys Leu Asp Lys Asn Pro Asn Leu Gly Glu Asp 100 105 110 Gln Ala Glu Glu Ile Ser Asp Glu Leu Met Glu Phe Ser Leu Lys Asp 115 120 125 Gln Glu Ala Lys Val Ser Arg Ser Gly Leu Tyr Arg Ser Pro Ser Met 130 135 140 Pro Glu Asn Leu Asn Arg Pro Arg Leu Lys Gln Val Glu Lys Phe Lys 145 150 155 160 Asp Asn Thr Ile Pro Asp Lys Val Lys Lys Lys Tyr Phe Ser Gly Gln 165 170 175 Gly Lys Leu Arg Lys Gly Leu Cys Leu Lys Lys Thr Val Ser Leu Cys 180 185 190 Asp Ile Thr Ile Thr Gln Met Leu Glu Glu Asp Ser Asn Gln Gly His 195 200 205 Leu Ile Gly Asp Phe Ser Lys Val Cys Ala Leu Pro Thr Val Ser Gly 210 215 220 Lys His Gln Asp Leu Lys Tyr Val Asn Pro Glu Thr Val Ala Ala Leu 225 230 235 240 Leu Ser Gly Lys Phe Gln Gly Leu Ile Glu Lys Phe Tyr Val Ile Asp 245 250 255 Cys Arg Tyr Pro Tyr Glu Tyr Leu Gly Gly His Ile Gln Gly Ala Leu 260 265 270 Asn Leu Tyr Ser Gln Glu Glu Leu Phe Asn Phe Phe Leu Lys Lys Pro 275 280 285 Ile Val Pro Leu Asp Thr Gln Lys Arg Ile Ile Ile Val Phe His Cys 290 295 300 Glu Phe Ser Ser Glu Arg Gly Pro Arg Met Cys Arg Cys Leu Arg Glu 305 310 315 320 Glu Asp Arg Ser Leu Asn Gln Tyr Pro Ala Leu Tyr Tyr Pro Glu Leu 325 330 335 Tyr Ile Leu Lys Gly Gly Tyr Arg Asp Phe Phe Pro Glu Tyr Met Glu 340 345 350 Leu Cys Glu Pro Gln Ser Tyr Cys Pro Met His His Gln Asp His Lys 355 360 365 Thr Glu Leu Leu Arg Cys Arg Ser Gln Ser Lys Val Gln Glu Gly Glu 370 375 380 Arg Gln Leu Arg Glu Gln Ile Ala Leu Leu Val Lys Asp Met Ser Pro 385 390 395 400 <210> SEQ ID NO 816 <211> LENGTH: 3318 <212> TYPE: DNA <213> ORGANISM: Homo sapiens <400> SEQUENCE: 816 gtgatgcgta gttccggctg ccggttgaca tgaagaagca gcagcggcta gggcggcggt 60 agctgcaggg gtcggggatt gcagcgggcc tcggggctaa gagcgcgacg cggcctagag 120 cggcagacgg cgcagtgggc cgagaaggag gcgcagcagc cgccctggcc cgtcatggag 180 atggaaaagg agttcgagca gatcgacaag tccgggagct gggcggccat ttaccaggat 240 atccgacatg aagccagtga cttcccatgt agagtggcca agcttcctaa gaacaaaaac 300 cgaaataggt acagagacgt cagtcccttt gaccatagtc ggattaaact acatcaagaa 360 gataatgact atatcaacgc tagtttgata aaaatggaag aagcccaaag gagttacatt 420 cttacccagg gccctttgcc taacacatgc ggtcactttt gggagatggt gtgggagcag 480 aaaagcaggg gtgtcgtcat gctcaacaga gtgatggaga aaggttcgtt aaaatgcgca 540 caatactggc cacaaaaaga agaaaaagag atgatctttg aagacacaaa tttgaaatta 600 acattgatct ctgaagatat caagtcatat tatacagtgc gacagctaga attggaaaac 660 cttacaaccc aagaaactcg agagatctta catttccact ataccacatg gcctgacttt 720 ggagtccctg aatcaccagc ctcattcttg aactttcttt tcaaagtccg agagtcaggg 780 tcactcagcc cggagcacgg gcccgttgtg gtgcactgca gtgcaggcat cggcaggtct 840 ggaaccttct gtctggctga tacctgcctc ttgctgatgg acaagaggaa agacccttct 900 tccgttgata tcaagaaagt gctgttagaa atgaggaagt ttcggatggg gctgatccag 960 acagccgacc agctgcgctt ctcctacctg gctgtgatcg aaggtgccaa attcatcatg 1020 ggggactctt ccgtgcagga tcagtggaag gagctttccc acgaggacct ggagccccca 1080 cccgagcata tccccccacc tccccggcca cccaaacgaa tcctggagcc acacaatggg 1140 aaatgcaggg agttcttccc aaatcaccag tgggtgaagg aagagaccca ggaggataaa 1200 gactgcccca tcaaggaaga aaaaggaagc cccttaaatg ccgcacccta cggcatcgaa 1260 agcatgagtc aagacactga agttagaagt cgggtcgtgg ggggaagtct tcgaggtgcc 1320 caggctgcct ccccagccaa aggggagccg tcactgcccg agaaggacga ggaccatgca 1380 ctgagttact ggaagccctt cctggtcaac atgtgcgtgg ctacggtcct cacggccggc 1440 gcttacctct gctacaggtt cctgttcaac agcaacacat agcctgaccc tcctccactc 1500 cacctccacc cactgtccgc ctctgcccgc agagcccacg cccgactagc aggcatgccg 1560 cggtaggtaa gggccgccgg accgcgtaga gagccgggcc ccggacggac gttggttctg 1620 cactaaaacc catcttcccc ggatgtgtgt ctcacccctc atccttttac tttttgcccc 1680 ttccactttg agtaccaaat ccacaagcca ttttttgagg agagtgaaag agagtaccat 1740 gctggcggcg cagagggaag gggcctacac ccgtcttggg gctcgcccca cccagggctc 1800 cctcctggag catcccaggc gggcggcacg ccaacagccc cccccttgaa tctgcaggga 1860 gcaactctcc actccatatt tatttaaaca attttttccc caaaggcatc catagtgcac 1920 tagcattttc ttgaaccaat aatgtattaa aattttttga tgtcagcctt gcatcaaggg 1980 ctttatcaaa aagtacaata ataaatcctc aggtagtact gggaatggaa ggctttgcca 2040 tgggcctgct gcgtcagacc agtactggga aggaggacgg ttgtaagcag ttgttattta 2100 gtgatattgt gggtaacgtg agaagataga acaatgctat aatatataat gaacacgtgg 2160 gtatttaata agaaacatga tgtgagatta ctttgtcccg cttattctcc tccctgttat 2220 ctgctagatc tagttctcaa tcactgctcc cccgtgtgta ttagaatgca tgtaaggtct 2280 tcttgtgtcc tgatgaaaaa tatgtgcttg aaatgagaaa ctttgatctc tgcttactaa 2340 tgtgccccat gtccaagtcc aacctgcctg tgcatgacct gatcattaca tggctgtggt 2400 tcctaagcct gttgctgaag tcattgtcgc tcagcaatag ggtgcagttt tccaggaata 2460 ggcatttgcc taattcctgg catgacactc tagtgacttc ctggtgaggc ccagcctgtc 2520 ctggtacagc agggtcttgc tgtaactcag acattccaag ggtatgggaa gccatattca 2580 cacctcacgc tctggacatg atttagggaa gcagggacac cccccgcccc ccacctttgg 2640 gatcagcctc cgccattcca agtcaacact cttcttgagc agaccgtgat ttggaagaga 2700 ggcacctgct ggaaaccaca cttcttgaaa cagcctgggt gacggtcctt taggcagcct 2760 gccgccgtct ctgtcccggt tcaccttgcc gagagaggcg cgtctgcccc accctcaaac 2820 cctgtggggc ctgatggtgc tcacgactct tcctgcaaag ggaactgaag acctccacat 2880 taagtggctt tttaacatga aaaacacggc agctgtagct cccgagctac tctcttgcca 2940 gcattttcac attttgcctt tctcgtggta gaagccagta cagagaaatt ctgtggtggg 3000 aacattcgag gtgtcaccct gcagagctat ggtgaggtgt ggataaggct taggtgccag 3060 gctgtaagca ttctgagctg ggcttgttgt ttttaagtcc tgtatatgta tgtagtagtt 3120 tgggtgtgta tatatagtag catttcaaaa tggacgtact ggtttaacct cctatccttg 3180 gagagcagct ggctctccac cttgttacac attatgttag agaggtagcg agctgctctg 3240 ctatatgcct taagccaata tttactcatc aggtcattat tttttacaat ggccatggaa 3300 taaaccattt ttacaaaa 3318 <210> SEQ ID NO 817 <211> LENGTH: 435 <212> TYPE: PRT <213> ORGANISM: Homo sapiens <400> SEQUENCE: 817 Met Glu Met Glu Lys Glu Phe Glu Gln Ile Asp Lys Ser Gly Ser Trp 1 5 10 15 Ala Ala Ile Tyr Gln Asp Ile Arg His Glu Ala Ser Asp Phe Pro Cys 20 25 30 Arg Val Ala Lys Leu Pro Lys Asn Lys Asn Arg Asn Arg Tyr Arg Asp 35 40 45 Val Ser Pro Phe Asp His Ser Arg Ile Lys Leu His Gln Glu Asp Asn 50 55 60 Asp Tyr Ile Asn Ala Ser Leu Ile Lys Met Glu Glu Ala Gln Arg Ser 65 70 75 80 Tyr Ile Leu Thr Gln Gly Pro Leu Pro Asn Thr Cys Gly His Phe Trp 85 90 95 Glu Met Val Trp Glu Gln Lys Ser Arg Gly Val Val Met Leu Asn Arg 100 105 110 Val Met Glu Lys Gly Ser Leu Lys Cys Ala Gln Tyr Trp Pro Gln Lys 115 120 125 Glu Glu Lys Glu Met Ile Phe Glu Asp Thr Asn Leu Lys Leu Thr Leu 130 135 140 Ile Ser Glu Asp Ile Lys Ser Tyr Tyr Thr Val Arg Gln Leu Glu Leu 145 150 155 160 Glu Asn Leu Thr Thr Gln Glu Thr Arg Glu Ile Leu His Phe His Tyr 165 170 175 Thr Thr Trp Pro Asp Phe Gly Val Pro Glu Ser Pro Ala Ser Phe Leu 180 185 190 Asn Phe Leu Phe Lys Val Arg Glu Ser Gly Ser Leu Ser Pro Glu His 195 200 205 Gly Pro Val Val Val His Cys Ser Ala Gly Ile Gly Arg Ser Gly Thr 210 215 220 Phe Cys Leu Ala Asp Thr Cys Leu Leu Leu Met Asp Lys Arg Lys Asp 225 230 235 240 Pro Ser Ser Val Asp Ile Lys Lys Val Leu Leu Glu Met Arg Lys Phe 245 250 255 Arg Met Gly Leu Ile Gln Thr Ala Asp Gln Leu Arg Phe Ser Tyr Leu 260 265 270 Ala Val Ile Glu Gly Ala Lys Phe Ile Met Gly Asp Ser Ser Val Gln 275 280 285 Asp Gln Trp Lys Glu Leu Ser His Glu Asp Leu Glu Pro Pro Pro Glu 290 295 300 His Ile Pro Pro Pro Pro Arg Pro Pro Lys Arg Ile Leu Glu Pro His 305 310 315 320 Asn Gly Lys Cys Arg Glu Phe Phe Pro Asn His Gln Trp Val Lys Glu 325 330 335 Glu Thr Gln Glu Asp Lys Asp Cys Pro Ile Lys Glu Glu Lys Gly Ser 340 345 350 Pro Leu Asn Ala Ala Pro Tyr Gly Ile Glu Ser Met Ser Gln Asp Thr 355 360 365 Glu Val Arg Ser Arg Val Val Gly Gly Ser Leu Arg Gly Ala Gln Ala 370 375 380 Ala Ser Pro Ala Lys Gly Glu Pro Ser Leu Pro Glu Lys Asp Glu Asp 385 390 395 400 His Ala Leu Ser Tyr Trp Lys Pro Phe Leu Val Asn Met Cys Val Ala 405 410 415 Thr Val Leu Thr Ala Gly Ala Tyr Leu Cys Tyr Arg Phe Leu Phe Asn 420 425 430 Ser Asn Thr 435 <210> SEQ ID NO 818 <211> LENGTH: 2346 <212> TYPE: DNA <213> ORGANISM: Mus musculus <400> SEQUENCE: 818 gaattcggga tccttttgca cattcctagt tagcagtgca tactcatcag actggagatg 60 tttaatgaca tcagggaacc aaacggacaa cccatagtac ccgaagacag ggtgaaccag 120 acaatcgtaa gcttgatggt gttttccctg actgggtagt tgaagcatct catgaatgtc 180 agccaaattc cgtacagttc ggtgcggatc cgaacgaaac acctcctgta ccaggttccc 240 gtgtcgctct caatttcaat cagctcatct atttgtttgg gagtcttgat tttatttacc 300 gtgaagacct tctctggctg gccccgggct ctcatgttgg tgtcatgaat taacttcaga 360 atcatccagg cttcatcatg ttttcccacc tccagcaaga accgagggct ttctggcatg 420 aaggtgagag ccaccacaga ggagacgcat gggagcgcac agacgatgac gaagacgcgc 480 cacgtgtgga actggtaggc tgaacccatg ctgaagctcc acccgtagtg gggaatgatg 540 gcccaggcat ggcggaggct agatgccgcc aatcatccag aacatgcaga agccgctgct 600 ggggagcttg gggctgcggt ggtggcgggt gacgggcttc gggacgcgga gcgacgcggc 660 ctagcgcggc ggacggccgt gggaactcgg gcagccgacc cgtcccgcca tggagatgga 720 gaaggagttc gaggagatcg acaaggctgg gaactgggcg gctatttacc aggacattcg 780 acatgaagcc agcgacttcc catgcaaagt cgcgaagctt cctaagaaca aaaaccggaa 840 caggtaccga gatgtcagcc cttttgacca cagtcggatt aaattgcacc aggaagataa 900 tgactatatc aatgccagct tgataaaaat ggaagaagcc cagaggagct atattctcac 960 ccagggccct ttaccaaaca catgtgggca cttctgggag atggtgtggg agcagaagag 1020 caggggcgtg gtcatgctca accgcatcat ggagaaaggc tcgttaaaat gtgcccagta 1080 ttggccacag caagaagaaa aggagatggt ctttgatgac acaggtttga agttgacact 1140 aatctctgaa gatgtcaagt catattacac agtacgacag ttggagttgg aaaacctgac 1200 taccaaggag actcgagaga tcctgcattt ccactacacc acatggcctg actttggagt 1260 ccccgagtca ccggcttctt tcctcaattt ccttttcaaa gtccgagagt caggctcact 1320 cagcctggag catggcccca ttgtggtcca ctgcagcgcc ggcatcggga ggtcagggac 1380 cttctgtctg gctgacacct gcctcttact gatggacaag aggaaagacc catcttccgt 1440 ggacatcaag aaagtactgc tggagatgcg caggttccgc atggggctca tccagactgc 1500 cgaccagctg cgcttctcct acctggctgt catcgagggc gccaagttca tcatgggcga 1560 ctcgtcagtg caggatcagt ggaaggagct ctcccgggag gatctagacc ttccacccga 1620 gcacgtgccc ccacctcccc ggccacccaa acgcacactg gagcctcaca acgggaagtg 1680 caaggagctc ttctccagcc accagtgggt gagcgaggag acctgtgggg atgaagacag 1740 cctggccaga gaggaaggca gagcccagtc aagtgccatg cacagcgtga gcagcatgag 1800 tccagacact gaagttagga gacggatggt gggtggaggt cttcaaagtg ctcaggcgtc 1860 tgtccccacc gaggaagagc tgtcctccac tgaggaggaa cacaaggcac attggccaag 1920 tcactggaag cccttcctgg tcaatgtgtg catggccacg ctcctggcca ccggcgcgta 1980 cttgtgctac cgggtgtgtt ttcactgaca gactgggagg cactgccact gcccagctta 2040 ggatgcggtc tgcggcgtct gacctggtgt agagggaaca acaactcgca agcctgctct 2100 ggaactggaa gggcctgccc caggagggta ttagtgcact gggctttgaa ggagcccctg 2160 gtcccacgaa cagagtctaa tctcagggcc ttaacctgtt caggagaagt agaggaaatg 2220 ccaaatactc ttcttgctct cacctcactc ctcccctttc tctgattcat ttgtttttgg 2280 aaaaaaaaaa aaaaagaatt acaacacatt gttgttttta acatttataa aggcaggccc 2340 gaattc 2346 <210> SEQ ID NO 819 <211> LENGTH: 432 <212> TYPE: PRT <213> ORGANISM: Mus musculus <400> SEQUENCE: 819 Met Glu Met Glu Lys Glu Phe Glu Glu Ile Asp Lys Ala Gly Asn Trp 1 5 10 15 Ala Ala Ile Tyr Gln Asp Ile Arg His Glu Ala Ser Asp Phe Pro Cys 20 25 30 Lys Val Ala Lys Leu Pro Lys Asn Lys Asn Arg Asn Arg Tyr Arg Asp 35 40 45 Val Ser Pro Phe Asp His Ser Arg Ile Lys Leu His Gln Glu Asp Asn 50 55 60 Asp Tyr Ile Asn Ala Ser Leu Ile Lys Met Glu Glu Ala Gln Arg Ser 65 70 75 80 Tyr Ile Leu Thr Gln Gly Pro Leu Pro Asn Thr Cys Gly His Phe Trp 85 90 95 Glu Met Val Trp Glu Gln Lys Ser Arg Gly Val Val Met Leu Asn Arg 100 105 110 Ile Met Glu Lys Gly Ser Leu Lys Cys Ala Gln Tyr Trp Pro Gln Gln 115 120 125 Glu Glu Lys Glu Met Val Phe Asp Asp Thr Gly Leu Lys Leu Thr Leu 130 135 140 Ile Ser Glu Asp Val Lys Ser Tyr Tyr Thr Val Arg Gln Leu Glu Leu 145 150 155 160 Glu Asn Leu Thr Thr Lys Glu Thr Arg Glu Ile Leu His Phe His Tyr 165 170 175 Thr Thr Trp Pro Asp Phe Gly Val Pro Glu Ser Pro Ala Ser Phe Leu 180 185 190 Asn Phe Leu Phe Lys Val Arg Glu Ser Gly Ser Leu Ser Leu Glu His 195 200 205 Gly Pro Ile Val Val His Cys Ser Ala Gly Ile Gly Arg Ser Gly Thr 210 215 220 Phe Cys Leu Ala Asp Thr Cys Leu Leu Leu Met Asp Lys Arg Lys Asp 225 230 235 240 Pro Ser Ser Val Asp Ile Lys Lys Val Leu Leu Glu Met Arg Arg Phe 245 250 255 Arg Met Gly Leu Ile Gln Thr Ala Asp Gln Leu Arg Phe Ser Tyr Leu 260 265 270 Ala Val Ile Glu Gly Ala Lys Phe Ile Met Gly Asp Ser Ser Val Gln 275 280 285 Asp Gln Trp Lys Glu Leu Ser Arg Glu Asp Leu Asp Leu Pro Pro Glu 290 295 300 His Val Pro Pro Pro Pro Arg Pro Pro Lys Arg Thr Leu Glu Pro His 305 310 315 320 Asn Gly Lys Cys Lys Glu Leu Phe Ser Ser His Gln Trp Val Ser Glu 325 330 335 Glu Thr Cys Gly Asp Glu Asp Ser Leu Ala Arg Glu Glu Gly Arg Ala 340 345 350 Gln Ser Ser Ala Met His Ser Val Ser Ser Met Ser Pro Asp Thr Glu 355 360 365 Val Arg Arg Arg Met Val Gly Gly Gly Leu Gln Ser Ala Gln Ala Ser 370 375 380 Val Pro Thr Glu Glu Glu Leu Ser Ser Thr Glu Glu Glu His Lys Ala 385 390 395 400 His Trp Pro Ser His Trp Lys Pro Phe Leu Val Asn Val Cys Met Ala 405 410 415 Thr Leu Leu Ala Thr Gly Ala Tyr Leu Cys Tyr Arg Val Cys Phe His 420 425 430 <210> SEQ ID NO 820 <211> LENGTH: 4127 <212> TYPE: DNA <213> ORGANISM: Rattus novegicus <400> SEQUENCE: 820 agccgctgct ggggaggttg gggctgaggt ggtggcgggc gacgggcctc gagacgcgga 60 gcgacgcggc ctagcgcggc ggacggccga gggaactcgg gcagtcgtcc cgtcccgcca 120 tggaaatgga gaaggaattc gagcagatcg ataaggctgg gaactgggcg gctatttacc 180 aggatattcg acatgaagcc agtgacttcc catgcagaat agcgaaactt cctaagaaca 240 aaaaccggaa caggtaccga gatgtcagcc cttttgacca cagtcggatt aaattgcatc 300 aggaagataa tgactatatc aatgccagct tgataaaaat ggaggaagcc cagaggagct 360 atatcctcac ccagggccct ttaccaaaca cgtgcgggca cttctgggag atggtgtggg 420 agcagaagag caggggcgtg gtcatgctca accgcatcat ggagaaaggc tcgttaaaat 480 gtgcccagta ttggccacag aaagaagaaa aagagatggt cttcgatgac accaatttga 540 agctgacact gatctctgaa gatgtcaagt catattacac agtacggcag ttggagttgg 600 agaacctggc tacccaggag gctcgagaga tcctgcattt ccactacacc acctggcctg 660 actttggagt ccctgagtca cctgcctctt tcctcaattt cctattcaaa gtccgagagt 720 caggctcact cagcccagag cacggcccca ttgtggtcca ctgcagtgct ggcattggca 780 ggtcagggac cttctgcctg gctgacacct gcctcttact gatggacaag aggaaagacc 840 cgtcctctgt ggacatcaag aaagtgctgt tggagatgcg caggttccgc atggggctca 900 tccagacggc cgaccaactg cgcttctcct acctggctgt gatcgagggt gcaaagttca 960 tcatgggcga ctcgtcagtg caggatcagt ggaaggagct ttcccatgaa gacctggagc 1020 ctccccctga gcacgtgccc ccacctcccc ggccacccaa acgcacattg gagcctcaca 1080 atggcaagtg caaggagctc ttctccaacc accagtgggt gagcgaggag agctgtgagg 1140 atgaggacat cctggccaga gaggaaagca gagccccctc aattgctgtg cacagcatga 1200 gcagtatgag tcaagacact gaagttagga aacggatggt gggtggaggt cttcaaagtg 1260 ctcaggcatc tgtccccact gaggaagagc tgtccccaac cgaggaggaa caaaaggcac 1320 acaggccagt tcactggaag cccttcctgg tcaacgtgtg catggccacg gccctggcga 1380 ctggcgcgta cctctgttac cgggtatgtt ttcactgaca gactgctgtg aggcatgagc 1440 gtggtgggcg ctgccactgc ccaggttagg atttggtctg cggcgtctaa cctggtgtag 1500 aagaaacaac agcttacaag cctgtggtgg aactggaagg gccagcccca ggaggggcat 1560 ctgtgcactg ggctttgaag gagcccctgg tcccaagaac agagtctaat ctcagggcct 1620 taacctgttc aggagaagta gaggaaatgc caaatactct tcttgctctc acctcactcc 1680 tcccctttct ctggttcgtt tgtttttgga aaaaaaaaaa aaagaattac aacacattgt 1740 tgtttttaac atttataaag gcaggttttt gttattttta gagaaaacaa aagatgctag 1800 gcactggtga gattctcttg tgccctttgg catgtgatca gattcacgat ttacgtttat 1860 ttccggggga gggtcccacc tgtcaggact gtaaagttcc tgctggcttg gtcagccccc 1920 ccaccccccc accccgagct tgcaggtgcc ctgctgtgag gagagcagca gcagaggctg 1980 cccctggaca gaagcccagc tctgcttccc tcaggtgtcc ctgcgtttcc atcctccttc 2040 tttgtgaccg ccatcttgca gatgacccag tcctcagcac cccacccctg cagatgggtt 2100 tctccgaggg cctgcctcag ggtcatcaga ggttggctgc cagcttagag ctggggcttc 2160 catttgattg gaaagtcatt actattctat gtagaagcca ctccactgag gtgtaaagca 2220 agactcataa aggaggagcc ttggtgtcat ggaagtcact ccgcgcgcag gacctgtaac 2280 aacctctgaa acactcagtc ctgctgcagt gacgtccttg aaggcatcag acagatgatt 2340 tgcagactgc caagacttgt cctgagccgt gatttttaga gtctggactc atgaaacacc 2400 gccgagcgct tactgtgcag cctctgatgc tggttggctg aggctgcggg gaggtggaca 2460 ctgtgggtgc atccagtgca gttgcttttg tgcagttggg tccagcagca cagcccgcac 2520 tccagcctca gctgcaggcc acagtggcca tggaggccgc cagagcgagc tggggtggat 2580 gcttgttcac ttggagcagc cttcccagga cgtgcagctc ccttcctgct ttgtccttct 2640 gcttccttcc ctggagtagc aagcccacga gcaatcgtga ggggtgtgag ggagctgcag 2700 aggcatcaga gtggcctgca gcggcgtgag gccccttccc ctccgacacc cccctccaga 2760 ggagccgctc cactgttatt tattcacttt gcccacagac acccctgagt gagcacaccc 2820 tgaaactgac cgtgtaaggt gtcagcctgc acccaggacc gtcaggtgca gcaccgggtc 2880 agtcctaggg ttgaggtagg actgacacag ccactgtgtg gctggtgctg gggcaggggc 2940 aggagctgag ggtcttagaa gcaatcttca ggaacagaca acagtggtga catgtaaagt 3000 ccctgtggct actgatgaca tgtgtaggat gaaggctggc ctttctccca tgactttcta 3060 gatcccgttc cccgtctgct ttccctgtga gttagaaaac acacaggctc ctgtcctggt 3120 ggtgccgtgt gcttgacatg ggaaacttag atgcctgctc actggcgggc acctcggcat 3180 cgccaccact cagagtgaga gcagtgctgt ccagtgccga ggccgcctga ctcccggcag 3240 gactcttcag gctctggcct gccccagcac accccgctgg atctcagaca ttccacaccc 3300 acacctcatt ccctggacac ttgggcaagc aggcccgccc ttccacctct ggggtcagcc 3360 cctccattcc gagttcacac tgctctggag caggccagga ccggaagcaa ggcagctggt 3420 gaggagcacc ctcctgggaa cagtgtaggt gacagtcctg agagtcagct tgctagcgct 3480 gctggcacca gtcaccttgc tcagaagtgt gtggctcttg aggctgaaga gactgatgat 3540 ggtgctcatg actcttctgt gaggggaact tgaccttcac attgggtggc tttttttaaa 3600 ataagcgaag gcagctggaa ctccagtctg cctcttgcca gcacttcaca ttttgccttt 3660 cacccagaga agccagcaca gagccactgg ggaaggcgat ggccttgcct gcacaggctg 3720 aggagatggc tcagccggcg tccaggctgt gtctggagca gggggtgcac agcagcctca 3780 caggtggggg cctcagagca ggcgctgccc tgtcccctgc cccgctggag gcagcaaagc 3840 tgctgcatgc cttaagtcaa tacttactca gcagggcgct ctcgttctct ctctctctct 3900 ctctctctct ctctctctct ctctctctct ctctaaatgg ccatagaata aaccatttta 3960 caaaaataaa agccaacaac aaagtgctct ggaatagcac ctttgcagga gcggggggtg 4020 tctcagggtc ttctgtgacc tcaccgaact gtccgactgc accgtttcca acttgtgtct 4080 cactaatggg tctgcattag ttgcaacaat aaatgttttt aaagaac 4127 <210> SEQ ID NO 821 <211> LENGTH: 432 <212> TYPE: PRT <213> ORGANISM: Rattus norvegicus <400> SEQUENCE: 821 Met Glu Met Glu Lys Glu Phe Glu Gln Ile Asp Lys Ala Gly Asn Trp 1 5 10 15 Ala Ala Ile Tyr Gln Asp Ile Arg His Glu Ala Ser Asp Phe Pro Cys 20 25 30 Arg Ile Ala Lys Leu Pro Lys Asn Lys Asn Arg Asn Arg Tyr Arg Asp 35 40 45 Val Ser Pro Phe Asp His Ser Arg Ile Lys Leu His Gln Glu Asp Asn 50 55 60 Asp Tyr Ile Asn Ala Ser Leu Ile Lys Met Glu Glu Ala Gln Arg Ser 65 70 75 80 Tyr Ile Leu Thr Gln Gly Pro Leu Pro Asn Thr Cys Gly His Phe Trp 85 90 95 Glu Met Val Trp Glu Gln Lys Ser Arg Gly Val Val Met Leu Asn Arg 100 105 110 Ile Met Glu Lys Gly Ser Leu Lys Cys Ala Gln Tyr Trp Pro Gln Lys 115 120 125 Glu Glu Lys Glu Met Val Phe Asp Asp Thr Asn Leu Lys Leu Thr Leu 130 135 140 Ile Ser Glu Asp Val Lys Ser Tyr Tyr Thr Val Arg Gln Leu Glu Leu 145 150 155 160 Glu Asn Leu Ala Thr Gln Glu Ala Arg Glu Ile Leu His Phe His Tyr 165 170 175 Thr Thr Trp Pro Asp Phe Gly Val Pro Glu Ser Pro Ala Ser Phe Leu 180 185 190 Asn Phe Leu Phe Lys Val Arg Glu Ser Gly Ser Leu Ser Pro Glu His 195 200 205 Gly Pro Ile Val Val His Cys Ser Ala Gly Ile Gly Arg Ser Gly Thr 210 215 220 Phe Cys Leu Ala Asp Thr Cys Leu Leu Leu Met Asp Lys Arg Lys Asp 225 230 235 240 Pro Ser Ser Val Asp Ile Lys Lys Val Leu Leu Glu Met Arg Arg Phe 245 250 255 Arg Met Gly Leu Ile Gln Thr Ala Asp Gln Leu Arg Phe Ser Tyr Leu 260 265 270 Ala Val Ile Glu Gly Ala Lys Phe Ile Met Gly Asp Ser Ser Val Gln 275 280 285 Asp Gln Trp Lys Glu Leu Ser His Glu Asp Leu Glu Pro Pro Pro Glu 290 295 300 His Val Pro Pro Pro Pro Arg Pro Pro Lys Arg Thr Leu Glu Pro His 305 310 315 320 Asn Gly Lys Cys Lys Glu Leu Phe Ser Asn His Gln Trp Val Ser Glu 325 330 335 Glu Ser Cys Glu Asp Glu Asp Ile Leu Ala Arg Glu Glu Ser Arg Ala 340 345 350 Pro Ser Ile Ala Val His Ser Met Ser Ser Met Ser Gln Asp Thr Glu 355 360 365 Val Arg Lys Arg Met Val Gly Gly Gly Leu Gln Ser Ala Gln Ala Ser 370 375 380 Val Pro Thr Glu Glu Glu Leu Ser Pro Thr Glu Glu Glu Gln Lys Ala 385 390 395 400 His Arg Pro Val His Trp Lys Pro Phe Leu Val Asn Val Cys Met Ala 405 410 415 Thr Ala Leu Ala Thr Gly Ala Tyr Leu Cys Tyr Arg Val Cys Phe His 420 425 430 <210> SEQ ID NO 822 <211> LENGTH: 2287 <212> TYPE: DNA <213> ORGANISM: Homo sapiens <400> SEQUENCE: 822 ggggggcctg agcctctccg ccggcgcagg ctctgctcgc gccagctcgc tcccgcagcc 60 atgcccacca ccatcgagcg ggagttcgaa gagttggata ctcagcgtcg ctggcagccg 120 ctgtacttgg aaattcgaaa tgagtcccat gactatcctc atagagtggc caagtttcca 180 gaaaacagaa atcgaaacag atacagagat gtaagcccat atgatcacag tcgtgttaaa 240 ctgcaaaatg ctgagaatga ttatattaat gccagtttag ttgacataga agaggcacaa 300 aggagttaca tcttaacaca gggtccactt cctaacacat gctgccattt ctggcttatg 360 gtttggcagc agaagaccaa agcagttgtc atgctgaacc gcattgtgga gaaagaatcg 420 gttaaatgtg cacagtactg gccaacagat gaccaagaga tgctgtttaa agaaacagga 480 ttcagtgtga agctcttgtc agaagatgtg aagtcgtatt atacagtaca tctactacaa 540 ttagaaaata tcaatagtgg tgaaaccaga acaatatctc actttcatta tactacctgg 600 ccagattttg gagtccctga atcaccagct tcatttctca atttcttgtt taaagtgaga 660 gaatctggct ccttgaaccc tgaccatggg cctgcggtga tccactgtag tgcaggcatt 720 gggcgctctg gcaccttctc tctggtagac acttgtcttg ttttgatgga aaaaggagat 780 gatattaaca taaaacaagt gttactgaac atgagaaaat accgaatggg tcttattcag 840 accccagatc aactgagatt ctcatacatg gctataatag aaggagcaaa atgtataaag 900 ggagattcta gtatacagaa acgatggaaa gaactttcta aggaagactt atctcctgcc 960 tttgatcatt caccaaacaa aataatgact gaaaaataca atgggaacag aataggtcta 1020 gaagaagaaa aactgacagg tgaccgatgt acaggacttt cctctaaaat gcaagataca 1080 atggaggaga acagtgagag tgctctacgg aaacgtattc gagaggacag aaaggccacc 1140 acagctcaga aggtgcagca gatgaaacag aggctaaatg agaatgaacg aaaaagaaaa 1200 aggtggttat attggcaacc tattctcact aagatggggt ttatgtcagt cattttggtt 1260 ggcgcttttg ttggctggag actgtttttt cagcaaaatg ccctataaac aattaatttt 1320 gcccagcaag cttctgcact agtaactgac agtgctacat taatcatagg ggtttgtctg 1380 cagcaaacgc ctcatatccc aaaaacggtg cagtagaata gacatcaacc agataagtga 1440 tatttacagt cacaagccca acatctcagg actcttgact gcaggttcct ctgaacccca 1500 aactgtaaat ggctgtctaa aataaagaca ttcatgtttg ttaaaaactg gtaaattttg 1560 caactgtatt catacatgtc aaacacagta tttcacctga ccaacattga gatatccttt 1620 atcacaggat ttgtttttgg aggctatctg gattttaacc tgcacttgat ataagcaata 1680 aatattgtgg ttttatctac gttattggaa agaaaatgac atttaaataa tgtgtgtaat 1740 gtataatgta ctattgacat gggcatcaac acttttattc ttaagcattt cagggtaaat 1800 atattttata agtatctatt taatcttttg tagttaactg tactttttaa gagctcaatt 1860 tgaaaaatct gttactaaaa aaaaaaattg tatgtcgatt gaattgtact ggatacattt 1920 tccatttttc taaaaagaag tttgatatga gcagttagaa gttggaataa gcaatttcta 1980 ctatatattg catttctttt atgttttaca gttttcccca ttttaaaaag aaaagcaaac 2040 aaagaaacaa aagtttttcc taaaaatatc tttgaaggaa aattctcctt actgggatag 2100 tcaggtaaac agttggtcaa gactttgtaa agaaattggt ttctgtaaat cccattattg 2160 atatgtttat ttttcatgaa aatttcaatg tagttggggt agattatgat ttaggaagca 2220 aaagtaagaa gcagcatttt atgattcata atttcagttt actagactga agttttgaag 2280 taaaccc 2287 <210> SEQ ID NO 823 <211> LENGTH: 415 <212> TYPE: PRT <213> ORGANISM: Homo sapiens <400> SEQUENCE: 823 Met Pro Thr Thr Ile Glu Arg Glu Phe Glu Glu Leu Asp Thr Gln Arg 1 5 10 15 Arg Trp Gln Pro Leu Tyr Leu Glu Ile Arg Asn Glu Ser His Asp Tyr 20 25 30 Pro His Arg Val Ala Lys Phe Pro Glu Asn Arg Asn Arg Asn Arg Tyr 35 40 45 Arg Asp Val Ser Pro Tyr Asp His Ser Arg Val Lys Leu Gln Asn Ala 50 55 60 Glu Asn Asp Tyr Ile Asn Ala Ser Leu Val Asp Ile Glu Glu Ala Gln 65 70 75 80 Arg Ser Tyr Ile Leu Thr Gln Gly Pro Leu Pro Asn Thr Cys Cys His 85 90 95 Phe Trp Leu Met Val Trp Gln Gln Lys Thr Lys Ala Val Val Met Leu 100 105 110 Asn Arg Ile Val Glu Lys Glu Ser Val Lys Cys Ala Gln Tyr Trp Pro 115 120 125 Thr Asp Asp Gln Glu Met Leu Phe Lys Glu Thr Gly Phe Ser Val Lys 130 135 140 Leu Leu Ser Glu Asp Val Lys Ser Tyr Tyr Thr Val His Leu Leu Gln 145 150 155 160 Leu Glu Asn Ile Asn Ser Gly Glu Thr Arg Thr Ile Ser His Phe His 165 170 175 Tyr Thr Thr Trp Pro Asp Phe Gly Val Pro Glu Ser Pro Ala Ser Phe 180 185 190 Leu Asn Phe Leu Phe Lys Val Arg Glu Ser Gly Ser Leu Asn Pro Asp 195 200 205 His Gly Pro Ala Val Ile His Cys Ser Ala Gly Ile Gly Arg Ser Gly 210 215 220 Thr Phe Ser Leu Val Asp Thr Cys Leu Val Leu Met Glu Lys Gly Asp 225 230 235 240 Asp Ile Asn Ile Lys Gln Val Leu Leu Asn Met Arg Lys Tyr Arg Met 245 250 255 Gly Leu Ile Gln Thr Pro Asp Gln Leu Arg Phe Ser Tyr Met Ala Ile 260 265 270 Ile Glu Gly Ala Lys Cys Ile Lys Gly Asp Ser Ser Ile Gln Lys Arg 275 280 285 Trp Lys Glu Leu Ser Lys Glu Asp Leu Ser Pro Ala Phe Asp His Ser 290 295 300 Pro Asn Lys Ile Met Thr Glu Lys Tyr Asn Gly Asn Arg Ile Gly Leu 305 310 315 320 Glu Glu Glu Lys Leu Thr Gly Asp Arg Cys Thr Gly Leu Ser Ser Lys 325 330 335 Met Gln Asp Thr Met Glu Glu Asn Ser Glu Ser Ala Leu Arg Lys Arg 340 345 350 Ile Arg Glu Asp Arg Lys Ala Thr Thr Ala Gln Lys Val Gln Gln Met 355 360 365 Lys Gln Arg Leu Asn Glu Asn Glu Arg Lys Arg Lys Arg Trp Leu Tyr 370 375 380 Trp Gln Pro Ile Leu Thr Lys Met Gly Phe Met Ser Val Ile Leu Val 385 390 395 400 Gly Ala Phe Val Gly Trp Arg Leu Phe Phe Gln Gln Asn Ala Leu 405 410 415 <210> SEQ ID NO 824 <211> LENGTH: 2477 <212> TYPE: DNA <213> ORGANISM: Homo sapiens <400> SEQUENCE: 824 gctcgggcgc cgagtctgcg cgctgacgtc cgacgctcca ggtactttcc ccacggccga 60 cagggcttgg cgtgggggcg gggcgcggcg cgcagcgcgc atgcgccgca gcgccagcgc 120 tctccccgga tcgtgcgggg cctgagcctc tccgccggcg caggctctgc tcgcgccagc 180 tcgctcccgc agccatgccc accaccatcg agcgggagtt cgaagagttg gatactcagc 240 gtcgctggca gccgctgtac ttggaaattc gaaatgagtc ccatgactat cctcatagag 300 tggccaagtt tccagaaaac agaaatcgaa acagatacag agatgtaagc ccatatgatc 360 acagtcgtgt taaactgcaa aatgctgaga atgattatat taatgccagt ttagttgaca 420 tagaagaggc acaaaggagt tacatcttaa cacagggtcc acttcctaac acatgctgcc 480 atttctggct tatggtttgg cagcagaaga ccaaagcagt tgtcatgctg aaccgcattg 540 tggagaaaga atcggttaaa tgtgcacagt actggccaac agatgaccaa gagatgctgt 600 ttaaagaaac aggattcagt gtgaagctct tgtcagaaga tgtgaagtcg tattatacag 660 tacatctact acaattagaa aatatcaata gtggtgaaac cagaacaata tctcactttc 720 attatactac ctggccagat tttggagtcc ctgaatcacc agcttcattt ctcaatttct 780 tgtttaaagt gagagaatct ggctccttga accctgacca tgggcctgcg gtgatccact 840 gtagtgcagg cattgggcgc tctggcacct tctctctggt agacacttgt cttgttttga 900 tggaaaaagg agatgatatt aacataaaac aagtgttact gaacatgaga aaataccgaa 960 tgggtcttat tcagacccca gatcaactga gattctcata catggctata atagaaggag 1020 caaaatgtat aaagggagat tctagtatac agaaacgatg gaaagaactt tctaaggaag 1080 acttatctcc tgcctttgat cattcaccaa acaaaataat gactgaaaaa tacaatggga 1140 acagaatagg tctagaagaa gaaaaactga caggtgaccg atgtacagga ctttcctcta 1200 aaatgcaaga tacaatggag gagaacagtg agagtgctct acggaaacgt attcgagagg 1260 acagaaaggc caccacagct cagaaggtgc agcagatgaa acagaggcta aatgagaatg 1320 aacgaaaaag aaaaaggtgg ttatattggc aacctattct cactaagatg gggtttatgt 1380 cagtcatttt ggttggcgct tttgttggct ggagactgtt ttttcagcaa aatgccctat 1440 aaacaattaa ttttgcccag caagcttctg cactagtaac tgacagtgct acattaatca 1500 taggggtttg tctgcagcaa acgcctcata tcccaaaaac ggtgcagtag aatagacatc 1560 aaccagataa gtgatattta cagtcacaag cccaacatct caggactctt gactgcaggt 1620 tcctctgaac cccaaactgt aaatggctgt ctaaaataaa gacattcatg tttgttaaaa 1680 actggtaaat tttgcaactg tattcataca tgtcaaacac agtatttcac ctgaccaaca 1740 ttgagatatc ctttatcaca ggatttgttt ttggaggcta tctggatttt aacctgcact 1800 tgatataagc aataaatatt gtggttttat ctacgttatt ggaaagaaaa tgacatttaa 1860 ataatgtgtg taatgtataa tgtactattg acatgggcat caacactttt attcttaagc 1920 atttcagggt aaatatattt tataagtatc tatttaatct tttgtagtta actgtacttt 1980 ttaagagctc aatttgaaaa atctgttact aaaaaaaaaa attgtatgtc gattgaattg 2040 tactggatac attttccatt tttctaaaaa gaagtttgat atgagcagtt agaagttgga 2100 ataagcaatt tctactatat attgcatttc ttttatgttt tacagttttc cccattttaa 2160 aaagaaaagc aaacaaagaa acaaaagttt ttcctaaaaa tatctttgaa ggaaaattct 2220 ccttactggg atagtcaggt aaacagttgg tcaagacttt gtaaagaaat tggtttctgt 2280 aaatcccatt attgatatgt ttatttttca tgaaaatttc aatgtagttg gggtagatta 2340 tgatttagga agcaaaagta agaagcagca ttttatgatt cataatttca gtttactaga 2400 ctgaagtttt gaagtaaaca cttttcagtt tctttctact tcaataaata gtatgattat 2460 atgcaaacct taaaaaa 2477 <210> SEQ ID NO 825 <211> LENGTH: 415 <212> TYPE: PRT <213> ORGANISM: Homo sapiens <400> SEQUENCE: 825 Met Pro Thr Thr Ile Glu Arg Glu Phe Glu Glu Leu Asp Thr Gln Arg 1 5 10 15 Arg Trp Gln Pro Leu Tyr Leu Glu Ile Arg Asn Glu Ser His Asp Tyr 20 25 30 Pro His Arg Val Ala Lys Phe Pro Glu Asn Arg Asn Arg Asn Arg Tyr 35 40 45 Arg Asp Val Ser Pro Tyr Asp His Ser Arg Val Lys Leu Gln Asn Ala 50 55 60 Glu Asn Asp Tyr Ile Asn Ala Ser Leu Val Asp Ile Glu Glu Ala Gln 65 70 75 80 Arg Ser Tyr Ile Leu Thr Gln Gly Pro Leu Pro Asn Thr Cys Cys His 85 90 95 Phe Trp Leu Met Val Trp Gln Gln Lys Thr Lys Ala Val Val Met Leu 100 105 110 Asn Arg Ile Val Glu Lys Glu Ser Val Lys Cys Ala Gln Tyr Trp Pro 115 120 125 Thr Asp Asp Gln Glu Met Leu Phe Lys Glu Thr Gly Phe Ser Val Lys 130 135 140 Leu Leu Ser Glu Asp Val Lys Ser Tyr Tyr Thr Val His Leu Leu Gln 145 150 155 160 Leu Glu Asn Ile Asn Ser Gly Glu Thr Arg Thr Ile Ser His Phe His 165 170 175 Tyr Thr Thr Trp Pro Asp Phe Gly Val Pro Glu Ser Pro Ala Ser Phe 180 185 190 Leu Asn Phe Leu Phe Lys Val Arg Glu Ser Gly Ser Leu Asn Pro Asp 195 200 205 His Gly Pro Ala Val Ile His Cys Ser Ala Gly Ile Gly Arg Ser Gly 210 215 220 Thr Phe Ser Leu Val Asp Thr Cys Leu Val Leu Met Glu Lys Gly Asp 225 230 235 240 Asp Ile Asn Ile Lys Gln Val Leu Leu Asn Met Arg Lys Tyr Arg Met 245 250 255 Gly Leu Ile Gln Thr Pro Asp Gln Leu Arg Phe Ser Tyr Met Ala Ile 260 265 270 Ile Glu Gly Ala Lys Cys Ile Lys Gly Asp Ser Ser Ile Gln Lys Arg 275 280 285 Trp Lys Glu Leu Ser Lys Glu Asp Leu Ser Pro Ala Phe Asp His Ser 290 295 300 Pro Asn Lys Ile Met Thr Glu Lys Tyr Asn Gly Asn Arg Ile Gly Leu 305 310 315 320 Glu Glu Glu Lys Leu Thr Gly Asp Arg Cys Thr Gly Leu Ser Ser Lys 325 330 335 Met Gln Asp Thr Met Glu Glu Asn Ser Glu Ser Ala Leu Arg Lys Arg 340 345 350 Ile Arg Glu Asp Arg Lys Ala Thr Thr Ala Gln Lys Val Gln Gln Met 355 360 365 Lys Gln Arg Leu Asn Glu Asn Glu Arg Lys Arg Lys Arg Trp Leu Tyr 370 375 380 Trp Gln Pro Ile Leu Thr Lys Met Gly Phe Met Ser Val Ile Leu Val 385 390 395 400 Gly Ala Phe Val Gly Trp Arg Leu Phe Phe Gln Gln Asn Ala Leu 405 410 415 <210> SEQ ID NO 826 <211> LENGTH: 1714 <212> TYPE: DNA <213> ORGANISM: Homo sapiens <400> SEQUENCE: 826 gctcgggcgc cgagtctgcg cgctgacgtc cgacgctcca ggtactttcc ccacggccga 60 cagggcttgg cgtgggggcg gggcgcggcg cgcagcgcgc atgcgccgca gcgccagcgc 120 tctccccgga tcgtgcgggg cctgagcctc tccgccggcg caggctctgc tcgcgccagc 180 tcgctcccgc agccatgccc accaccatcg agcgggagtt cgaagagttg gatactcagc 240 gtcgctggca gccgctgtac ttggaaattc gaaatgagtc ccatgactat cctcatagag 300 tggccaagtt tccagaaaac agaaatcgaa acagatacag agatgtaagc ccatatgatc 360 acagtcgtgt taaactgcaa aatgctgaga atgattatat taatgccagt ttagttgaca 420 tagaagaggc acaaaggagt tacatcttaa cacagggtcc acttcctaac acatgctgcc 480 atttctggct tatggtttgg cagcagaaga ccaaagcagt tgtcatgctg aaccgcattg 540 tggagaaaga atcggttaaa tgtgcacagt actggccaac agatgaccaa gagatgctgt 600 ttaaagaaac aggattcagt gtgaagctct tgtcagaaga tgtgaagtcg tattatacag 660 tacatctact acaattagaa aatatcaata gtggtgaaac cagaacaata tctcactttc 720 attatactac ctggccagat tttggagtcc ctgaatcacc agcttcattt ctcaatttct 780 tgtttaaagt gagagaatct ggctccttga accctgacca tgggcctgcg gtgatccact 840 gtagtgcagg cattgggcgc tctggcacct tctctctggt agacacttgt cttgttttga 900 tggaaaaagg agatgatatt aacataaaac aagtgttact gaacatgaga aaataccgaa 960 tgggtcttat tcagacccca gatcaactga gattctcata catggctata atagaaggag 1020 caaaatgtat aaagggagat tctagtatac agaaacgatg gaaagaactt tctaaggaag 1080 acttatctcc tgcctttgat cattcaccaa acaaaataat gactgaaaaa tacaatggga 1140 acagaatagg tctagaagaa gaaaaactga caggtgaccg atgtacagga ctttcctcta 1200 aaatgcaaga tacaatggag gagaacagtg agagtgctct acggaaacgt attcgagagg 1260 acagaaaggc caccacagct cagaaggtgc agcagatgaa acagaggcta aatgagaatg 1320 aacgaaaaag aaaaaggcca agattgacag acacctaata ttcatgactt gagaatattc 1380 tgcagctata aattttgaac cattgatgtg caaagcaaga cctgaagccc actccggaaa 1440 ctaaagtgag gctcgctaac cctctagatt gcctcacagt tgtttgttta caaagtaaac 1500 tttacatcca ggggatgaag agcacccacc agcagaagac tttgcagaac ctttaattgg 1560 atgtgttaag tgtttttaat gagtgtatga aatgtagaaa gatgtacaag aaataaatta 1620 ggagagatta ctttgtattg tactgccatt cctactgtat ttttatactt tttggcagca 1680 ttaaatattt ttgttaaata aaaaaaaaaa aaaa 1714 <210> SEQ ID NO 827 <211> LENGTH: 387 <212> TYPE: PRT <213> ORGANISM: Homo sapiens <400> SEQUENCE: 827 Met Pro Thr Thr Ile Glu Arg Glu Phe Glu Glu Leu Asp Thr Gln Arg 1 5 10 15 Arg Trp Gln Pro Leu Tyr Leu Glu Ile Arg Asn Glu Ser His Asp Tyr 20 25 30 Pro His Arg Val Ala Lys Phe Pro Glu Asn Arg Asn Arg Asn Arg Tyr 35 40 45 Arg Asp Val Ser Pro Tyr Asp His Ser Arg Val Lys Leu Gln Asn Ala 50 55 60 Glu Asn Asp Tyr Ile Asn Ala Ser Leu Val Asp Ile Glu Glu Ala Gln 65 70 75 80 Arg Ser Tyr Ile Leu Thr Gln Gly Pro Leu Pro Asn Thr Cys Cys His 85 90 95 Phe Trp Leu Met Val Trp Gln Gln Lys Thr Lys Ala Val Val Met Leu 100 105 110 Asn Arg Ile Val Glu Lys Glu Ser Val Lys Cys Ala Gln Tyr Trp Pro 115 120 125 Thr Asp Asp Gln Glu Met Leu Phe Lys Glu Thr Gly Phe Ser Val Lys 130 135 140 Leu Leu Ser Glu Asp Val Lys Ser Tyr Tyr Thr Val His Leu Leu Gln 145 150 155 160 Leu Glu Asn Ile Asn Ser Gly Glu Thr Arg Thr Ile Ser His Phe His 165 170 175 Tyr Thr Thr Trp Pro Asp Phe Gly Val Pro Glu Ser Pro Ala Ser Phe 180 185 190 Leu Asn Phe Leu Phe Lys Val Arg Glu Ser Gly Ser Leu Asn Pro Asp 195 200 205 His Gly Pro Ala Val Ile His Cys Ser Ala Gly Ile Gly Arg Ser Gly 210 215 220 Thr Phe Ser Leu Val Asp Thr Cys Leu Val Leu Met Glu Lys Gly Asp 225 230 235 240 Asp Ile Asn Ile Lys Gln Val Leu Leu Asn Met Arg Lys Tyr Arg Met 245 250 255 Gly Leu Ile Gln Thr Pro Asp Gln Leu Arg Phe Ser Tyr Met Ala Ile 260 265 270 Ile Glu Gly Ala Lys Cys Ile Lys Gly Asp Ser Ser Ile Gln Lys Arg 275 280 285 Trp Lys Glu Leu Ser Lys Glu Asp Leu Ser Pro Ala Phe Asp His Ser 290 295 300 Pro Asn Lys Ile Met Thr Glu Lys Tyr Asn Gly Asn Arg Ile Gly Leu 305 310 315 320 Glu Glu Glu Lys Leu Thr Gly Asp Arg Cys Thr Gly Leu Ser Ser Lys 325 330 335 Met Gln Asp Thr Met Glu Glu Asn Ser Glu Ser Ala Leu Arg Lys Arg 340 345 350 Ile Arg Glu Asp Arg Lys Ala Thr Thr Ala Gln Lys Val Gln Gln Met 355 360 365 Lys Gln Arg Leu Asn Glu Asn Glu Arg Lys Arg Lys Arg Pro Arg Leu 370 375 380 Thr Asp Thr 385 <210> SEQ ID NO 828 <211> LENGTH: 1555 <212> TYPE: DNA <213> ORGANISM: Mus musculus <400> SEQUENCE: 828 tctccccgga tagagcgggg cccgagcctg tccgctgtgg tagttccgct cggctgcccc 60 gccgccatgt cggcaaccat cgagcgggag ttcgaggaac tggatgctca gtgtcgctgg 120 cagccgttat acttggaaat tcgaaatgaa tcccatgact atcctcatag agtggccaag 180 tttccagaaa acagaaaccg aaacagatac agagatgtaa gcccatatga tcacagtcgt 240 gttaaactgc aaagtactga aaatgattat attaatgcca gcttagttga catagaagag 300 gcacaaagaa gttacatctt aacacagggc ccacttccga acacatgctg ccatttctgg 360 ctcatggtgt ggcagcaaaa gaccaaagca gttgtcatgc taaaccgaac tgtagaaaaa 420 gaatcggtta aatgtgcaca gtactggcca acggatgaca gagaaatggt gtttaaggaa 480 acgggattca gtgtgaagct cttatctgaa gatgtaaaat catattatac agtacatcta 540 ctacagttag aaaatatcaa tactggtgaa acgagaacca tatctcactt ccattatacc 600 acctggccag attttggggt tccagagtca ccagcttcat ttctaaactt cttgtttaaa 660 gttagagaat ctggttgttt gacccctgac catggacctg cagtgatcca ttgcagtgcg 720 ggcatcgggc gctctggcac cttctctctt gtagatacct gtcttgttct gatggaaaaa 780 ggagaggatg ttaatgtgaa acaattatta ctgaatatga gaaagtatcg aatgggactt 840 attcagacac cggaccaact cagattctcc tacatggcca taatagaagg agcaaagtac 900 acaaaaggag attcaaatat acagaaacgg tggaaagaac tttctaaaga agatttatct 960 cctatttgtg atcattcaca gaacagagtg atggttgaga agtacaatgg gaagagaata 1020 ggttcagaag atgaaaagtt aacagggctt ccttctaagg tgcaggatac tgtggaggag 1080 agcagtgaga gcattctacg gaaacgtatt cgagaggata gaaaggctac gacggctcag 1140 aaggtgcagc agatgaaaca gaggctaaat gaaactgaac gaaaaagaaa aaggccaaga 1200 ttgacagaca cctaaatgtt catgacttga gactattctg cagctataaa atttgaacct 1260 ttgatgtgca aagcaagacc tgaagcccac tccggaaact aaagtgaggc ttgctaaccc 1320 tgtagattgc ctcacaagtt gtctgtttac aaagtaagct ttccatccag gggatgaaga 1380 acgccaccag cagaagactt gcaaaccctt taatttgatg tattgttttt taacatgtgt 1440 atgaaatgta gaaagatgta aaggaaataa attaggagcg actactttgt attgtactgc 1500 cattcctaat gtatttttat actttttggc agcattaaat atttttatta aatag 1555 <210> SEQ ID NO 829 <211> LENGTH: 382 <212> TYPE: PRT <213> ORGANISM: Mus musculus <400> SEQUENCE: 829 Met Ser Ala Thr Ile Glu Arg Glu Phe Glu Glu Leu Asp Ala Gln Cys 1 5 10 15 Arg Trp Gln Pro Leu Tyr Leu Glu Ile Arg Asn Glu Ser His Asp Tyr 20 25 30 Pro His Arg Val Ala Lys Phe Pro Glu Asn Arg Asn Arg Asn Arg Tyr 35 40 45 Arg Asp Val Ser Pro Tyr Asp His Ser Arg Val Lys Leu Gln Ser Thr 50 55 60 Glu Asn Asp Tyr Ile Asn Ala Ser Leu Val Asp Ile Glu Glu Ala Gln 65 70 75 80 Arg Ser Tyr Ile Leu Thr Gln Gly Pro Leu Pro Asn Thr Cys Cys His 85 90 95 Phe Trp Leu Met Val Trp Gln Gln Lys Thr Lys Ala Val Val Met Leu 100 105 110 Asn Arg Thr Val Glu Lys Glu Ser Val Lys Cys Ala Gln Tyr Trp Pro 115 120 125 Thr Asp Asp Arg Glu Met Val Phe Lys Glu Thr Gly Phe Ser Val Lys 130 135 140 Leu Leu Ser Glu Asp Val Lys Ser Tyr Tyr Thr Val His Leu Leu Gln 145 150 155 160 Leu Glu Asn Ile Asn Thr Gly Glu Thr Arg Thr Ile Ser His Phe His 165 170 175 Tyr Thr Thr Trp Pro Asp Phe Gly Val Pro Glu Ser Pro Ala Ser Phe 180 185 190 Leu Asn Phe Leu Phe Lys Val Arg Glu Ser Gly Cys Leu Thr Pro Asp 195 200 205 His Gly Pro Ala Val Ile His Cys Ser Ala Gly Ile Gly Arg Ser Gly 210 215 220 Thr Phe Ser Leu Val Asp Thr Cys Leu Val Leu Met Glu Lys Gly Glu 225 230 235 240 Asp Val Asn Val Lys Gln Leu Leu Leu Asn Met Arg Lys Tyr Arg Met 245 250 255 Gly Leu Ile Gln Thr Pro Asp Gln Leu Arg Phe Ser Tyr Met Ala Ile 260 265 270 Ile Glu Gly Ala Lys Tyr Thr Lys Gly Asp Ser Asn Ile Gln Lys Arg 275 280 285 Trp Lys Glu Leu Ser Lys Glu Asp Leu Ser Pro Ile Cys Asp His Ser 290 295 300 Gln Asn Arg Val Met Val Glu Lys Tyr Asn Gly Lys Arg Ile Gly Ser 305 310 315 320 Glu Asp Glu Lys Leu Thr Gly Leu Pro Ser Lys Val Gln Asp Thr Val 325 330 335 Glu Glu Ser Ser Glu Ser Ile Leu Arg Lys Arg Ile Arg Glu Asp Arg 340 345 350 Lys Ala Thr Thr Ala Gln Lys Val Gln Gln Met Lys Gln Arg Leu Asn 355 360 365 Glu Thr Glu Arg Lys Arg Lys Arg Pro Arg Leu Thr Asp Thr 370 375 380 <210> SEQ ID NO 830 <211> LENGTH: 1666 <212> TYPE: DNA <213> ORGANISM: Homo sapiens <400> SEQUENCE: 830 ggccccccgt tccccgccag gctgcaggcg tcgggcctgg gccgtcaggg cagctgtgac 60 cggatcgctt cccgggcggc gagctggggg tgcacccgga ccgccgcccc cgggatcatg 120 ggcaatggca tgaccaaggt acttcctgga ctctacctcg gaaacttcat tgatgccaaa 180 gacctggatc agctgggccg aaataagatc acacacatca tctctatcca tgagtcaccc 240 cagcctctgc tgcaggatat cacctacctt cgcatcccgg tcgctgatac ccctgaggta 300 cccatcaaaa agcacttcaa agaatgtatc aacttcatcc actgctgccg ccttaatggg 360 gggaactgcc ttgtgcactg ctttgcaggc atctctcgca gcaccacgat tgtgacagcg 420 tatgtgatga ctgtgacggg gctaggctgg cgggacgtgc ttgaagccat caaggccacc 480 aggcccatcg ccaaccccaa cccaggcttt aggcagcagc ttgaagagtt tggctgggcc 540 agttcccaga agggtgccag acataggacc tcaaaaacct ctggtgccca atgccctccg 600 atgacttcag caacctggat ggtcaccgga cccaaagtac cagatctgtc tgtgcttcgg 660 tgaggaggac ccgggcccca cacagcaccc caaggagcag ctcatcatgg cggacgtgca 720 ggtgcagctt cggcctggga gctcgtcctg cactctaagt gcctcaaccg agcgcccaga 780 tgggtcctca acccctggca accccgatgg catcactcac cttcaatgca gctgcctcca 840 tcctaagcga gccgcttcct cttcttgtac ccgctgaagg cagcccccaa caggggggct 900 ccctactccc acccaaccct gcccacacta agcccataga cttggggcct cccccggcac 960 atcacccagg tctgccggac ggcagaggtg gatcgcggcc ttccactcct ctgtcacggg 1020 gccccggaac tcgagagtag gccacaccgc cccccagctg ggcatggggc ttcggcagga 1080 aactgaactt gatcttgagg ccccagaaag gcagcaactg gagcagaagc aagacttcat 1140 ctcttgctga cagcccaatt tgtcaatagc gctttcctca gagccagcct taacctgctg 1200 ttgagtccat taaaacgttt gcttaaagtt tttaccaata attagatcat cagggttgtt 1260 tagtgtggga tcaagccata acaaaactgc ctagcctctc aggggcctag aatttacaga 1320 accttcctcc tccctgcagc aagtctctct tctttattct gggggctggg aaggatccca 1380 aaacagggaa cttggccgaa ccctgggctt tggatgctaa ccactgaagt accagcacct 1440 gtaggatgct gtctttgaag aaactgaggc ggacctccaa atgcagccct aaggcagagg 1500 tcaacgtgga agaccagccc ttctccaagc cccactggtc tttgcaagct gtacgttgta 1560 ggcaatctga gaactggaaa gggggactac aaccagaaag ttggttaccc tgccatggga 1620 ataaagtagc tgttttccac cccaaaaaaa aaaaaaaaaa aaaaaa 1666 <210> SEQ ID NO 831 <211> LENGTH: 181 <212> TYPE: PRT <213> ORGANISM: Homo sapiens <400> SEQUENCE: 831 Met Gly Asn Gly Met Thr Lys Val Leu Pro Gly Leu Tyr Leu Gly Asn 1 5 10 15 Phe Ile Asp Ala Lys Asp Leu Asp Gln Leu Gly Arg Asn Lys Ile Thr 20 25 30 His Ile Ile Ser Ile His Glu Ser Pro Gln Pro Leu Leu Gln Asp Ile 35 40 45 Thr Tyr Leu Arg Ile Pro Val Ala Asp Thr Pro Glu Val Pro Ile Lys 50 55 60 Lys His Phe Lys Glu Cys Ile Asn Phe Ile His Cys Cys Arg Leu Asn 65 70 75 80 Gly Gly Asn Cys Leu Val His Cys Phe Ala Gly Ile Ser Arg Ser Thr 85 90 95 Thr Ile Val Thr Ala Tyr Val Met Thr Val Thr Gly Leu Gly Trp Arg 100 105 110 Asp Val Leu Glu Ala Ile Lys Ala Thr Arg Pro Ile Ala Asn Pro Asn 115 120 125 Pro Gly Phe Arg Gln Gln Leu Glu Glu Phe Gly Trp Ala Ser Ser Gln 130 135 140 Lys Gly Ala Arg His Arg Thr Ser Lys Thr Ser Gly Ala Gln Cys Pro 145 150 155 160 Pro Met Thr Ser Ala Thr Trp Met Val Thr Gly Pro Lys Val Pro Asp 165 170 175 Leu Ser Val Leu Arg 180 <210> SEQ ID NO 832 <211> LENGTH: 1807 <212> TYPE: DNA <213> ORGANISM: Homo sapiens <400> SEQUENCE: 832 ggccccccgt tccccgccag gctgcaggcg tcgggcctgg gccgtcaggg cagctgtgac 60 cggatcgctt cccgggcggc gagctggggg tgcacccgga ccgccgcccc cgggatcatg 120 ggcaatggca tgaccaaggt acttcctgga ctctacctcg gaaacttcat tgatgccaaa 180 gacctggatc agctgggccg aaataagatc acacacatca tctctatcca tgagtcaccc 240 cagcctctgc tgcaggatat cacctacctt cgcatcccgg tcgctgatac ccctgaggta 300 cccatcaaaa agcacttcaa agaatgtatc aacttcatcc actgctgccg ccttaatggg 360 gggaactgcc ttgtgcactg ctttgcaggc atctctcgca gcaccacgat tgtgacagcg 420 tatgtgatga ctgtgacggg gctaggctgg cgggacgtgc ttgaagccat caaggccacc 480 aggcccatcg ccaaccccaa cccaggcttt aggcagcagc ttgaagagtt tggctgggcc 540 agttcccaga agggtgccag acataggacc tcaaaaacct ctggtgccca atgccctccg 600 atgacttcag caacctgcct gctggctgca cgtgtggctc ttctctccgc agcgctggtg 660 cgcgaagcca ccgggcgcac agcccagcgc tgtcgtctga gtccgcgggc ggccgccgag 720 cgcctgctgg ggccgccacc tcacgttgca gcaggatggt caccggaccc aaagtaccag 780 atctgtctgt gcttcggtga ggaggacccg ggccccacac agcaccccaa ggagcagctc 840 atcatggcgg acgtgcaggt gcagcttcgg cctgggagct cgtcctgcac tctaagtgcc 900 tcaaccgagc gcccagatgg gtcctcaacc cctggcaacc ccgatggcat cactcacctt 960 caatgcagct gcctccatcc taagcgagcc gcttcctctt cttgtacccg ctgaaggcag 1020 cccccaacag gggggctccc tactcccacc caaccctgcc cacactaagc ccatagactt 1080 ggggcctccc cggcggcaca tcacccaggt ctgccggacg gcagaggtgg atcgcggcct 1140 tccactcctc tgtcacgggg ccccggaact cgagagtagg ccacaccgcc ccccagctgg 1200 gcatggggct tcggcaggaa actgaacttg atcttgaggc cccagaaagg cagcaactgg 1260 agcagaagca agacttcatc tcttgctgac agcccaattt gtcaatagcg ctttcctcag 1320 agccagcctt aacctgctgt tgagtccatt aaaacgtttg cttaaagttt ttaccaataa 1380 ttagatcatc agggttgttt agtgtgggat caagccataa caaaactgcc tagcctctca 1440 ggggcctaga atttacagaa ccttcctcct ccctgcagct agtctctctt ctttattctg 1500 ggggctggga aggatcccaa aacagggaac ttggccgaac cctgggcttt ggatgctaac 1560 cactgaagta ccagcacctg taggatgctg tctttgaaga aactgaggcg gacctccaaa 1620 tgcagcccta aggcagaggt caacgtggaa gaccagccct tctccaagcc ccactggtct 1680 ttgcaagctg tacgttgtag gcaatctgag aactggaaag ggggactaca accagaaagt 1740 tggttaccct gccatgggaa taaagtagct gttttccacc ccaaaaaaaa aaaaaaaaaa 1800 aaaaaaa 1807 <210> SEQ ID NO 833 <211> LENGTH: 298 <212> TYPE: PRT <213> ORGANISM: Homo sapiens <400> SEQUENCE: 833 Met Gly Asn Gly Met Thr Lys Val Leu Pro Gly Leu Tyr Leu Gly Asn 1 5 10 15 Phe Ile Asp Ala Lys Asp Leu Asp Gln Leu Gly Arg Asn Lys Ile Thr 20 25 30 His Ile Ile Ser Ile His Glu Ser Pro Gln Pro Leu Leu Gln Asp Ile 35 40 45 Thr Tyr Leu Arg Ile Pro Val Ala Asp Thr Pro Glu Val Pro Ile Lys 50 55 60 Lys His Phe Lys Glu Cys Ile Asn Phe Ile His Cys Cys Arg Leu Asn 65 70 75 80 Gly Gly Asn Cys Leu Val His Cys Phe Ala Gly Ile Ser Arg Ser Thr 85 90 95 Thr Ile Val Thr Ala Tyr Val Met Thr Val Thr Gly Leu Gly Trp Arg 100 105 110 Asp Val Leu Glu Ala Ile Lys Ala Thr Arg Pro Ile Ala Asn Pro Asn 115 120 125 Pro Gly Phe Arg Gln Gln Leu Glu Glu Phe Gly Trp Ala Ser Ser Gln 130 135 140 Lys Gly Ala Arg His Arg Thr Ser Lys Thr Ser Gly Ala Gln Cys Pro 145 150 155 160 Pro Met Thr Ser Ala Thr Cys Leu Leu Ala Ala Arg Val Ala Leu Leu 165 170 175 Ser Ala Ala Leu Val Arg Glu Ala Thr Gly Arg Thr Ala Gln Arg Cys 180 185 190 Arg Leu Ser Pro Arg Ala Ala Ala Glu Arg Leu Leu Gly Pro Pro Pro 195 200 205 His Val Ala Ala Gly Trp Ser Pro Asp Pro Lys Tyr Gln Ile Cys Leu 210 215 220 Cys Phe Gly Glu Glu Asp Pro Gly Pro Thr Gln His Pro Lys Glu Gln 225 230 235 240 Leu Ile Met Ala Asp Val Gln Val Gln Leu Arg Pro Gly Ser Ser Ser 245 250 255 Cys Thr Leu Ser Ala Ser Thr Glu Arg Pro Asp Gly Ser Ser Thr Pro 260 265 270 Gly Asn Pro Asp Gly Ile Thr His Leu Gln Cys Ser Cys Leu His Pro 275 280 285 Lys Arg Ala Ala Ser Ser Ser Cys Thr Arg 290 295 <210> SEQ ID NO 834 <211> LENGTH: 1268 <212> TYPE: DNA <213> ORGANISM: Homo sapiens <400> SEQUENCE: 834 ggccccccgt tccccgccag gctgcaggcg tcgggcctgg gccgtcaggg cagctgtgac 60 cggatcgctt cccgggcggc gagctggggg tgcacccgga ccgccgcccc cgggatcatg 120 ggcaatggca tgaccaaggt acttcctgga ctctacctcg gaaacttcat tgatgccaaa 180 gacctggatc agctgggccg aaataagatc acacacatca tctctatcca tgagtcaccc 240 cagcctctgc tgcaggatat cacctacctt cgcatcccgg tcgctgatac ccctgaggta 300 cccatcaaaa agcacttcaa agaatgtatc aacttcatcc actgctgccg ccttaatggg 360 gggaactgcc ttgtgcactg ctttgcaggc atctctcgca gcaccacgat tgtgacagcg 420 tatgtgatga ctgtgacggg gctaggctgg cgggacgtgc ttgaagccat caaggccacc 480 aggcccatcg ccaaccccaa cccaggcttt aggcagcagc ttgaagagtt tggctgggcc 540 agttcccaga agggtgccag acataggacc tcaaaaacct ctggtgccca atgccctccg 600 atgacttcag caacctggat ggtcaccgga cccaaagtac cagatctgtc tgtgcttcgg 660 tgaggaggac ccgggcccca cacagcaccc caaggagcag ctcatcatgg cggacgtgca 720 ggtgcagctt cggcctggga gctcgtcctg cactctaagt gcctcaaccg agcgcccaga 780 tgggtcctca acccctggca accccgatgg catcactcac cttcaatgca gcttgcctcc 840 atcctaagcg agccgcttcc tcttcttgta cccgctgaag gcaagccccc aacagggggg 900 ctccctactc ccacccaacc ctgcccacac taagcccata gacttggggc ctcccccggc 960 acatcaccca ggtctgccgg acggcagagg tggatcgcgg ccttccactc ctctgtcacg 1020 gggccccgga actcgagagt aggcctcacc gccccccagc tgggcatggg gcttcggcag 1080 gaaactgaac ttgatcttga ggccagcaga aaggcagcaa ctggagcaga agcaagactt 1140 catctcttgc tgacagccca atttgtcaat agcgctttcc tcagagccag ccttaacctg 1200 ctgttgagtc cattaaaacg tttgcttaaa gtttttacca ataaaaaaaa aaaaaaaaaa 1260 aaaaaaaa 1268 <210> SEQ ID NO 835 <211> LENGTH: 181 <212> TYPE: PRT <213> ORGANISM: Homo sapiens <400> SEQUENCE: 835 Met Gly Asn Gly Met Thr Lys Val Leu Pro Gly Leu Tyr Leu Gly Asn 1 5 10 15 Phe Ile Asp Ala Lys Asp Leu Asp Gln Leu Gly Arg Asn Lys Ile Thr 20 25 30 His Ile Ile Ser Ile His Glu Ser Pro Gln Pro Leu Leu Gln Asp Ile 35 40 45 Thr Tyr Leu Arg Ile Pro Val Ala Asp Thr Pro Glu Val Pro Ile Lys 50 55 60 Lys His Phe Lys Glu Cys Ile Asn Phe Ile His Cys Cys Arg Leu Asn 65 70 75 80 Gly Gly Asn Cys Leu Val His Cys Phe Ala Gly Ile Ser Arg Ser Thr 85 90 95 Thr Ile Val Thr Ala Tyr Val Met Thr Val Thr Gly Leu Gly Trp Arg 100 105 110 Asp Val Leu Glu Ala Ile Lys Ala Thr Arg Pro Ile Ala Asn Pro Asn 115 120 125 Pro Gly Phe Arg Gln Gln Leu Glu Glu Phe Gly Trp Ala Ser Ser Gln 130 135 140 Lys Gly Ala Arg His Arg Thr Ser Lys Thr Ser Gly Ala Gln Cys Pro 145 150 155 160 Pro Met Thr Ser Ala Thr Trp Met Val Thr Gly Pro Lys Val Pro Asp 165 170 175 Leu Ser Val Leu Arg 180 <210> SEQ ID NO 836 <211> LENGTH: 1045 <212> TYPE: DNA <213> ORGANISM: Homo sapiens <400> SEQUENCE: 836 ggccccccgt tccccgccag gctgcaggcg tcgggcctgg gccgtcaggg cagctgtgac 60 cggatcgctt cccgggcggc gagctggggg tgcacccgga ccgccgcccc cgggatcatg 120 ggcaatggca tgaccaaggt acttcctgga ctctacctcg gaaacttcat tgatgccaaa 180 gacctggatc agctgggccg aaataagatc acacacatca tctctatcca tgagtcaccc 240 cagcctctgc tgcaggatat cacctacctt cgcatcccgg tcgctgatac ccctgaggta 300 cccatcaaaa agcacttcaa agaatgtatc aacttcatcc actgctgccg ccttaatggg 360 gggaactgcc ttgtgcactg ctttgcaggc atctctcgca gcaccacgat tgtgacagcg 420 tatgtgatga ctgtgacggg gctaggctgg cgggacgtgc ttgaagccat caaggccacc 480 aggcccatcg ccaaccccaa cccaggcttt aggcagcagc ttgaagagtt tggctgggcc 540 agttcccaga agggtgccag acataggacc tcaaaaacct ctggtgccca atgccctccg 600 atgacttcag caacctggat ggtcaccgga cccaaagtac cagatctgtc tgtgcttcgg 660 tgaggaggac ccgggcccca cacagcaccc caaggagcag ctcatcatgg cggacctagt 720 ctctcttctt tattctgggg gctgggaagg atcccaaaac agggaacttg gccgaaccct 780 gggctttgga tgctaaccac tgaagtacca gcacctgtag gatgctgtct ttgaagaaac 840 tgaggcggac ctccaaatgc agccctaagg cagaggtcaa cgtggaagac cagcccttct 900 ccaagcccca ctggtctttg caagctgtac gttgtaggca atctgagaac tggaaagggg 960 gactacaacc agaaagttgg ttaccctgcc atgggaataa agtagctgtt ttccacccca 1020 taaaaaaaaa aaaaaaaaaa aaaaa 1045 <210> SEQ ID NO 837 <211> LENGTH: 181 <212> TYPE: PRT <213> ORGANISM: Homo sapiens <400> SEQUENCE: 837 Met Gly Asn Gly Met Thr Lys Val Leu Pro Gly Leu Tyr Leu Gly Asn 1 5 10 15 Phe Ile Asp Ala Lys Asp Leu Asp Gln Leu Gly Arg Asn Lys Ile Thr 20 25 30 His Ile Ile Ser Ile His Glu Ser Pro Gln Pro Leu Leu Gln Asp Ile 35 40 45 Thr Tyr Leu Arg Ile Pro Val Ala Asp Thr Pro Glu Val Pro Ile Lys 50 55 60 Lys His Phe Lys Glu Cys Ile Asn Phe Ile His Cys Cys Arg Leu Asn 65 70 75 80 Gly Gly Asn Cys Leu Val His Cys Phe Ala Gly Ile Ser Arg Ser Thr 85 90 95 Thr Ile Val Thr Ala Tyr Val Met Thr Val Thr Gly Leu Gly Trp Arg 100 105 110 Asp Val Leu Glu Ala Ile Lys Ala Thr Arg Pro Ile Ala Asn Pro Asn 115 120 125 Pro Gly Phe Arg Gln Gln Leu Glu Glu Phe Gly Trp Ala Ser Ser Gln 130 135 140 Lys Gly Ala Arg His Arg Thr Ser Lys Thr Ser Gly Ala Gln Cys Pro 145 150 155 160 Pro Met Thr Ser Ala Thr Trp Met Val Thr Gly Pro Lys Val Pro Asp 165 170 175 Leu Ser Val Leu Arg 180 <210> SEQ ID NO 838 <211> LENGTH: 982 <212> TYPE: DNA <213> ORGANISM: Homo sapiens <400> SEQUENCE: 838 ggccccccgt tccccgccag gctgcaggcg tcgggcctgg gccgtcaggg cagctgtgac 60 cggatcgctt cccgggcggc gagctggggg tgcacccgga ccgccgcccc cgggatcatg 120 ggcaatggca tgaccaaggt acttcctgga ctctacctcg gaaacttcat tgatgccaaa 180 gacctggatc agctgggccg aaataagatc acacacatca tctctatcca tgagtcaccc 240 cagcctctgc tgcaggatat cacctacctt cgcatcccgg tcgctgatac ccctgaggta 300 cccatcaaaa agcacttcaa agaatgtatc aacttcatcc actgctgccg ccttaatggg 360 gggaactgcc ttgtgcactg ctttgcaggc atctctcgca gcaccacgat tgtgacagcg 420 tatgtgatga ctgtgacggg gctaggctgg cgggacgtgc ttgaagccat caaggccacc 480 aggcccatcg ccaaccccaa cccaggcttt aggcagcagc ttaagagttt ggctgggcca 540 gttcccagaa ggatggtcac cggacccaaa gtaccagatc tgtctgtgct tcggtgagga 600 ggacccgggc cccacacagc accccaagga gcagctcatc atggcggacc tagtctctct 660 tctttattct gggggctggg aaggatccca aaacagggaa cttggccgaa ccctgggctt 720 tggatgctaa ccactgaagt accagcacct gtaggatgct gtctttgaag aaactgaggc 780 ggacctccaa atgcagccct aaggcagagg tcaacgtgga agaccagccc ttctccaagc 840 cccactggtc tttgcaagct gtacgttgta ggcaatctga gaactggaaa gggggactac 900 aaccagaaag ttggttaccc tgccatggga ataaagtagc tgttttccac cccccaaaaa 960 aaaaaaaaaa aaaaaaaaaa aa 982 <210> SEQ ID NO 839 <211> LENGTH: 159 <212> TYPE: PRT <213> ORGANISM: Homo sapiens <400> SEQUENCE: 839 Met Gly Asn Gly Met Thr Lys Val Leu Pro Gly Leu Tyr Leu Gly Asn 1 5 10 15 Phe Ile Asp Ala Lys Asp Leu Asp Gln Leu Gly Arg Asn Lys Ile Thr 20 25 30 His Ile Ile Ser Ile His Glu Ser Pro Gln Pro Leu Leu Gln Asp Ile 35 40 45 Thr Tyr Leu Arg Ile Pro Val Ala Asp Thr Pro Glu Val Pro Ile Lys 50 55 60 Lys His Phe Lys Glu Cys Ile Asn Phe Ile His Cys Cys Arg Leu Asn 65 70 75 80 Gly Gly Asn Cys Leu Val His Cys Phe Ala Gly Ile Ser Arg Ser Thr 85 90 95 Thr Ile Val Thr Ala Tyr Val Met Thr Val Thr Gly Leu Gly Trp Arg 100 105 110 Asp Val Leu Glu Ala Ile Lys Ala Thr Arg Pro Ile Ala Asn Pro Asn 115 120 125 Pro Gly Phe Arg Gln Gln Leu Lys Ser Leu Ala Gly Pro Val Pro Arg 130 135 140 Arg Met Val Thr Gly Pro Lys Val Pro Asp Leu Ser Val Leu Arg 145 150 155 <210> SEQ ID NO 840 <211> LENGTH: 1064 <212> TYPE: DNA <213> ORGANISM: Homo sapiens <400> SEQUENCE: 840 ggccccccgt tccccgccag gctgcaggcg tcgggcctgg gccgtcaggg cagctgtgac 60 cggatcgctt cccgggcggc gagctggggg tgcacccgga ccgccgcccc cgggatcatg 120 ggcaatggca tgaccaaggt acttcctgga ctctacctcg gaaacttcat tgatgccaaa 180 gacctggatc agctgggccg aaataagatc acacacatca tctctatcca tgagtcaccc 240 cagcctctgc tgcaggatat cacctacctt cgcatcccgg tcgctgatac ccctgaggta 300 cccatcaaaa agcacttcaa agaatgtatc aacttcatcc actgctgccg ccttaatggg 360 gggaactgcc ttgtgcactg ctttgcaggc atctctcgca gcaccacgat tgtgacagcg 420 tatgtgatga ctgtgacggg gctaggctgg cgggacgtgc ttgaagccat caaggccacc 480 aggcccatcg ccaaccccaa cccaggcttt aggcagcagc ttgaagagtt tggctgggcc 540 agttcccaga agggctttta ccaacctcat aagctgttgt gagaaccaat tgagacactg 600 caggaaagtg tttagccagg cccagcactg atgagcagtc ggatggtcac cggacccaaa 660 gtaccagatc tgtctgtgct tcggtgagga ggacccgggc cccacacagc accccaagga 720 gcagctcatc atggcggacc tagtctctct tctttattct gggggctggg aaggatccca 780 aaacagggaa cttggccgaa ccctgggctt tggatgctaa ccactgaagt accagcacct 840 gtaggatgct gtctttgaag aaactgaggc ggacctccaa atgcagccct aaggcagagg 900 tcaacgtgga agaccagccc ttctccaagc cccactggtc tttgcaagct gtacgttgta 960 ggcaatctga gaactggaaa gggggactac aaccagaaag ttggttaccc tgccatggga 1020 ataaagtagc tgttttccaa aaaaaaaaaa aaaaaaaaaa aaaa 1064 <210> SEQ ID NO 841 <211> LENGTH: 154 <212> TYPE: PRT <213> ORGANISM: Homo sapiens <400> SEQUENCE: 841 Met Gly Asn Gly Met Thr Lys Val Leu Pro Gly Leu Tyr Leu Gly Asn 1 5 10 15 Phe Ile Asp Ala Lys Asp Leu Asp Gln Leu Gly Arg Asn Lys Ile Thr 20 25 30 His Ile Ile Ser Ile His Glu Ser Pro Gln Pro Leu Leu Gln Asp Ile 35 40 45 Thr Tyr Leu Arg Ile Pro Val Ala Asp Thr Pro Glu Val Pro Ile Lys 50 55 60 Lys His Phe Lys Glu Cys Ile Asn Phe Ile His Cys Cys Arg Leu Asn 65 70 75 80 Gly Gly Asn Cys Leu Val His Cys Phe Ala Gly Ile Ser Arg Ser Thr 85 90 95 Thr Ile Val Thr Ala Tyr Val Met Thr Val Thr Gly Leu Gly Trp Arg 100 105 110 Asp Val Leu Glu Ala Ile Lys Ala Thr Arg Pro Ile Ala Asn Pro Asn 115 120 125 Pro Gly Phe Arg Gln Gln Leu Glu Glu Phe Gly Trp Ala Ser Ser Gln 130 135 140 Lys Gly Phe Tyr Gln Pro His Lys Leu Leu 145 150 <210> SEQ ID NO 842 <211> LENGTH: 19 <212> TYPE: RNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: Small interfering RNA - PRL-3 <400> SEQUENCE: 842 agacccggug cugcguuau 19 

What is claimed is:
 1. An isolated small interfering RNA (siRNA) polynucleotide, comprising at least one nucleotide sequence selected from the group consisting of SEQ ID NOS:4-7, 100-103, 105-108, 120-123, 125-128, 130-133, 140-143, 145-148, 150-153, 440-443, 445-448, 455-458, 460-463, 465-468, 470-473, 475-478, 480-483, 485-488, and 490-493.
 2. The small interfering RNA polynucleotide of claim 1 that comprises at least one nucleotide sequence selected from the group consisting of SEQ ID NOS: 4-7, 100-103, 105-108, 120-123, 125-128, 130-133, 140-143, 145-148, 150-153, 440-443, 445-448, 455-458, 460-463, 465-468, 470-473, 475-478, 480-483, 485-488, and 490-493 and the complementary polynucleotide thereto.
 3. A small interfering RNA polynucleotide of either claim 1 or claim 2 that is capable of interfering with expression of a polypeptide, which polypeptide comprises an amino acid sequence as set forth in a sequence selected from the group consisting of SEQ ID NO: 779, SEQ ID NO:789, SEQ ID NO:791, SEQ ID NO:797, SEQ ID NO:799, SEQ ID NO:801, SEQ ID NO:803, SEQ ID NO:805, SEQ ID NO:807, SEQ ID NO:809, SEQ ID NO:811, and SEQ ID NO:813.
 4. The siRNA polynucleotide of either claim 1 or claim 2 wherein the nucleotide sequence of the siRNA polynucleotide differs by one, two, three or four nucleotides at any of positions 1-19 of a sequence selected from the group consisting of the sequences set forth in SEQ ID NOS: 4-7, 100-103, 105-108, 120-123, 125-128, 130-133, 140-143, 145-148, 150-153, 440-443, 445-448, 455-458, 460-463, 465-468, 470-473, 475-478, 480-483, 485-488, and 490-493.
 5. The siRNA polynucleotide of either claim 1 or claim 2 wherein the nucleotide sequence of the siRNA polynucleotide differs by at least two, three or four nucleotides at any of positions 1-19 of a sequence selected from the group consisting of the sequences set forth in SEQ ID NOS: 4-7, 100-103, 105-108, 120-123, 125-128, 130-133, 140-143, 145-148, 150-153, 440-443, 445-448, 455-458, 460-463, 465-468, 470-473, 475-478, 480-483, 485-488, and 490-493.
 6. An isolated siRNA polynucleotide comprising a nucleotide sequence according to SEQ ID NO: 4, or the complement thereof.
 7. An isolated siRNA polynucleotide comprising a nucleotide sequence selected from the group consisting of SEQ ID NOS: 100 and 105, or the complement thereof.
 8. An isolated siRNA polynucleotide comprising a nucleotide sequence selected from the group consisting of SEQ ID NOS: 120, 125, and 130, or the complement thereof.
 9. An isolated siRNA polynucleotide comprising a nucleotide sequence selected from the group consisting of SEQ ID NOS: 140, 145, and 150, or the complement thereof.
 10. An isolated siRNA polynucleotide comprising a nucleotide sequence selected from the group consisting of SEQ ID NOS: 440 and 445, or the complement thereof.
 11. An isolated siRNA polynucleotide comprising a nucleotide sequence selected from the group consisting of SEQ ID NOS: 455 and 460, or the complement thereof.
 12. An isolated siRNA polynucleotide comprising a nucleotide sequence according to SEQ ID NO: 465, or the complement thereof.
 13. An isolated siRNA polynucleotide comprising a nucleotide sequence selected from the group consisting of SEQ ID NOS: 470 and 475, or the complement thereof.
 14. An isolated siRNA polynucleotide comprising a nucleotide sequence selected from the group consisting of SEQ ID NOS: 480, 485, and 490, or the complement thereof.
 15. The siRNA polynucleotide of claim 1 or claim 2 wherein the polynucleotide comprises at least one synthetic nucleotide analogue of a naturally occurring nucleotide.
 16. The siRNA polynucleotide of claim 1 or claim 2 wherein the polynucleotide is linked to a detectable label.
 17. The siRNA polynucleotide of claim 16 wherein the detectable label is a reporter molecule.
 18. The siRNA of claim 17 wherein the reporter molecule is selected from the group consisting of a dye, a radionuclide, a luminescent group, a fluorescent group, and biotin.
 19. The siRNA polynucleotide of claim 18 wherein the fluorescent group is fluorescein isothiocyanate.
 20. The siRNA polynucleotide of claim 16 wherein the detectable label is a magnetic particle.
 21. A pharmaceutical composition comprising the siRNA polynucleotide of either claim 1 or claim 2 and a physiologically acceptable carrier.
 22. The pharmaceutical composition of claim 22 wherein the carrier comprises a liposome.
 23. A recombinant nucleic acid construct comprising a polynucleotide that is capable of directing transcription of a small interfering RNA (siRNA), the polynucleotide comprising: (i) a first promoter; (ii) a second promoter; and (iii) at least one DNA polynucleotide segment comprising at least one nucleotide sequence selected from the group consisting of SEQ ID NOS: 4-7, 100-103, 105-108, 120-123, 125-128, 130-133, 140-143, 145-148, 150-153, 440-443, 445-448, 455-458, 460-463, 465-468, 470-473, 475-478, 480-483, 485-488, and 490-493, or a complement thereto, wherein each DNA polynucleotide segment and its complement are operably linked to at least one of the first and second promoters, and wherein the promoters are oriented to direct transcription of the DNA polynucleotide segment and its reverse complement.
 24. The recombinant nucleic acid construct of claim 23, comprising at least one enhancer that is selected from a first enhancer operably linked to the first promoter and a second enhancer operably linked to the second promoter.
 25. The recombinant nucleic acid construct of claim 23, comprising at least one transcriptional terminator that is selected from (i) a first transcriptional terminator that is positioned in the construct to terminate transcription directed by the first promoter and (ii) a second transcriptional terminator that is positioned in the construct to terminate transcription directed by the second promoter.
 26. The recombinant nucleic acid construct of claim 24 wherein the siRNA is capable of interfering with expression of a polypeptide, wherein the polypeptide comprises an amino acid sequence as set forth in a sequence selected from the group consisting of SEQ ID NO: 779, SEQ ID NO:789, SEQ ID NO:791, SEQ ID NO:797, SEQ ID NO:799, SEQ ID NO:801, SEQ ID NO:803, SEQ ID NO:805, SEQ ID NO:807, SEQ ID NO:809, SEQ ID NO:811, and SEQ ID NO:813.
 27. A recombinant nucleic acid construct comprising a polynucleotide that is capable of directing transcription of a small interfering RNA (siRNA), the polynucleotide comprising at least one promoter and a DNA polynucleotide segment, wherein the DNA polynucleotide segment is operably linked to the promoter, and wherein the DNA polynucleotide segment comprises (i) at least one DNA polynucleotide that comprises at least one nucleotide sequence selected from the group consisting of SEQ ID NOS: 4-7, 100-103, 105-108, 120-123, 125-128, 130-133, 140-143, 145-148, 150-153, 440-443, 445-448, 455-458, 460-463, 465-468, 470-473, 475-478, 480-483, 485-488, and 490-493, or a complement thereto; (ii) a spacer sequence comprising at least 4 nucleotides operably linked to the DNA polynucleotide of (i); and (iii) the reverse complement of the DNA polynucleotide of (i) operably linked to the spacer sequence.
 28. The recombinant nucleic acid construct of claim 27 wherein the siRNA comprises an overhang of at least one and no more than four nucleotides, the overhang being located immediately 3′ to (iii).
 29. The recombinant nucleic acid construct of claim 27 wherein the spacer sequence comprises at least 9 nucleotides.
 30. The recombinant nucleic acid construct of claim 27 wherein the spacer sequence comprises two uridine nucleotides that are contiguous with (iii).
 31. The recombinant nucleic acid construct of claim 27 comprising at least one transcriptional terminator that is operably linked to the DNA polynucleotide segment.
 32. A host cell transformed or transfected with the recombinant nucleic acid construct of any one of claims 23-31.
 33. A pharmaceutical composition comprising an siRNA polynucleotide and a physiologically acceptable carrier, wherein the siRNA polynucleotide is selected from the group consisting of: (i) an RNA polynucleotide which comprises at least one nucleotide sequence selected from the group consisting of SEQ ID NOS: 4-7, 100-103, 105-108, 120-123, 125-128, 130-133, 140-143, 145-148, 150-153, 440-443, 445-448, 455-458, 460-463, 465-468, 470-473, 475-478, 480-483, 485-488, and 490-493, (ii) an RNA polynucleotide that comprises at least one nucleotide sequence selected from the group consisting of SEQ ID NOS: 4-7, 100-103, 105-108, 120-123, 125-128, 130-133, 140-143, 145-148, 150-153, 440-443, 445-448, 455-458, 460-463, 465-468, 470-473, 475-478, 480-483, 485-488, and 490-493 and the complementary polynucleotide thereto, (iii) an RNA polynucleotide according to (i) or (ii) wherein the nucleotide sequence of the siRNA polynucleotide differs by one, two or three nucleotides at any of positions 1-19 of a sequence selected from the group consisting of the sequences set forth in SEQ ID NOS: 4-7, 100-103, 105-108, 120-123, 125-128, 130-133, 140-143, 145-148, 150-153, 440-443, 445-448, 455-458, 460-463, 465-468, 470-473, 475-478, 480-483, 485-488, and 490-493, and (iv) an RNA polynucleotide according to (i) or (ii) wherein the nucleotide sequence of the siRNA polynucleotide differs by two, three or four nucleotides at any of positions 1-19 of a sequence selected from the group consisting of the sequences set forth in SEQ ID NOS: 4-7, 100-103, 105-108, 120-123, 125-128, 130-133, 140-143, 145-148, 150-153, 440-443, 445-448, 455-458, 460-463, 465-468, 470-473, 475-478, 480-483, 485-488, and 490-493.
 34. The pharmaceutical composition of claim 33 wherein the carrier comprises a liposome.
 35. A method for interfering with expression of a polypeptide, or variant thereof, comprising contacting a subject that comprises at least one cell which is capable of expressing the polypeptide with a siRNA polynucleotide for a time and under conditions sufficient to interfere with expression of the polypeptide, wherein: (a) the polypeptide comprises an amino acid sequence as set forth in a sequence selected from the group consisting of SEQ ID NO: 779, SEQ ID NO:789, SEQ ID NO:791, SEQ ID NO:797, SEQ ID NO:799, SEQ ID NO:801, SEQ ID NO:803, SEQ ID NO:805, SEQ ID NO:807, SEQ ID NO:809, SEQ ID NO:811, and SEQ ID NO:813, (b) the siRNA polynucleotide is selected from the group consisting of (i) an RNA polynucleotide which comprises at least one nucleotide sequence selected from the group consisting of SEQ ID NOS: 4-7, 100-103, 105-108, 120-123, 125-128, 130-133, 140-143, 145-148, 150-153, 440-443, 445-448, 455-458, 460-463, 465-468, 470-473, 475-478, 480-483, 485-488, and 490-493, (ii) an RNA polynucleotide that comprises at least one nucleotide sequence selected from the group consisting of SEQ ID NOS: 4-7, 100-103, 105-108, 120-123, 125-128, 130-133, 140-143, 145-148, 150-153, 440-443, 445-448, 455-458, 460-463, 465-468, 470-473, 475-478, 480-483, 485-488, and 490-493 and the complementary polynucleotide thereto, (iii) an RNA polynucleotide according to (i) or (ii) wherein the nucleotide sequence of the siRNA polynucleotide differs by one, two or three nucleotides at any of positions 1-19 of a sequence selected from the group consisting of the sequences set forth in SEQ ID NOS: 4-7, 100-103, 105-108, 120-123, 125-128, 130-133, 140-143, 145-148, 150-153, 440-443, 445-448, 455-458, 460-463, 465-468, 470-473, 475-478, 480-483, 485-488, and 490-493, and (iv) an RNA polynucleotide according to (i) or (ii) wherein the nucleotide sequence of the siRNA polynucleotide differs by two, three or four nucleotides at any of positions 1-19 of a sequence selected from the group consisting of the sequences set forth in SEQ ID NOS: 4-7, 100-103, 105-108, 120-123, 125-128, 130-133, 140-143, 145-148, 150-153, 440-443, 445-448, 455-458, 460-463, 465-468, 470-473, 475-478, 480-483, 485-488, and 490-493.
 36. A method for interfering with expression of a polypeptide that comprises an amino acid sequence as set forth in a sequence selected from the group consisting of SEQ ID NO: 779, SEQ ID NO:789, SEQ ID NO:791, SEQ ID NO:797, SEQ ID NO:799, SEQ ID NO:801, SEQ ID NO:803, SEQ ID NO:805, SEQ ID NO:807, SEQ ID NO:809, SEQ ID NO:811, and SEQ ID NO:813, or a variant of said polypeptide, said method comprising contacting, under conditions and for a time sufficient to interfere with expression of the polypeptide, (i) a subject that comprises at least one cell that is capable of expressing the polypeptide, and (ii) a recombinant nucleic acid construct according to either claim 23 or claim
 27. 37. A method for identifying a component of a signal transduction pathway comprising: A. contacting a siRNA polynucleotide and a first biological sample comprising at least one cell that is capable of expressing a target polypeptide, or a variant of said polypeptide, under conditions and for a time sufficient for target polypeptide expression when the siRNA polynucleotide is not present, wherein (1) the target polypeptide comprises an amino acid sequence as set forth in a sequence selected from the group consisting of SEQ ID NO: 779, SEQ ID NO: 789, SEQ ID NO: 791, SEQ ID NO: 797, SEQ ID NO: 799, SEQ ID NO: 801, SEQ ID NO: 803, SEQ ID NO: 805, SEQ ID NO: 807, SEQ ID NO: 809, SEQ ID NO: 811, and SEQ ID NO: 813, (2) the siRNA polynucleotide is selected from the group consisting of (i) an RNA polynucleotide which comprises at least one nucleotide sequence selected from the group consisting of SEQ ID NOS: 4-7, 100-103, 105-108, 120-123, 125-128, 130-133, 140-143, 145-148, 150-153, 440-443, 445-448, 455-458, 460-463, 465-468, 470-473, 475-478, 480-483, 485-488, and 490-493, (ii) an RNA polynucleotide that comprises at least one nucleotide sequence selected from the group consisting of SEQ ID NOS: 4-7, 100-103, 105-108, 120-123, 125-128, 130-133, 140-143, 145-148, 150-153, 440-443, 445-448, 455-458, 460-463, 465-468, 470-473, 475-478, 480-483, 485-488, and 490-493 and the complementary polynucleotide thereto, (iii) an RNA polynucleotide according to (i) or (ii) wherein the nucleotide sequence of the siRNA polynucleotide differs by one, two or three nucleotides at any of positions 1-19 of a sequence selected from the group consisting of the sequences set forth in SEQ ID NOS: 4-7, 100-103, 105-108, 120-123, 125-128, 130-133, 140-143, 145-148, 150-153, 440-443, 445-448, 455-458, 460-463, 465-468, 470-473, 475-478, 480-483, 485-488, and 490-493, and (iv) an RNA polynucleotide according to (i) or (ii) wherein the nucleotide sequence of the siRNA polynucleotide differs by two, three or four nucleotides at any of positions 1-19 of a sequence selected from the group consisting of the sequences set forth in SEQ ID NOS: 4-7, 100-103, 105-108, 120-123, 125-128, 130-133, 140-143, 145-148, 150-153, 440-443, 445-448, 455-458, 460-463, 465-468, 470-473, 475-478, 480-483, 485-488, and 490-493; and B. comparing a level of phosphorylation of at least one protein that is capable of being phosphorylated in the cell with a level of phosphorylation of the protein in a control sample that has not been contacted with the siRNA polynucleotide, wherein an altered level of phosphorylation of the protein in the presence of the siRNA polynucleotide relative to the level of phosphorylation of the protein in an absence of the siRNA polynucleotide indicates that the protein is a component of a signal transduction pathway. 